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NCT02154568
|
27:30:treatment
|
Any condition for which a MRI procedure is contraindicated
| 3
|
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NCT02332668
|
12:34:treatment
|
has failed prior standard therapy
| 3
|
[
"has",
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"therapy"
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0,
0,
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NCT00293475
|
12:59:cancer
|
high-grade primary central nervous system lymphoma (PCNSL) as documented by brain biopsy
| 3
|
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NCT01653093
|
,,,108:111:treatment
|
Patients must have an estimated glomerular filtration rate of >= 30 mL/min/1.73m^2 within six weeks of the MRI
| 3
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NCT02100891
|
1:11:cancer,23:45:cancer,82:108:treatment
|
CNS tumors: High risk malignant brain tumors that are recurrent or refractory to standard frontline therapy are eligible
| 3
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NCT02913495
|
1:16:chronic_disease
|
Placenta previa
| 3
|
[
"Placenta",
"previa"
] |
[
2,
2
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NCT02799095
|
,65:89:treatment,,
|
A female not of childbearing potential is one who has undergone bilateral oophorectomies or who is postmenopausal, defined as >45 years of age and without a menstrual period for 12 consecutive months
| 3
|
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NCT01810588
|
1:25:cancer
|
Myelodysplastic syndrome
| 3
|
[
"Myelodysplastic",
"syndrome"
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[
3,
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NCT01494324
|
22:30:treatment
|
Patients who are not surgical candidates
| 3
|
[
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0,
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NCT03100539
|
25:47:chronic_disease
|
Complex neck pain (e.g. cervical radiculopathy or recent whiplash injury)
| 3
|
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NCT02390752
|
1:5:treatment,,45:65:treatment,93:115:chronic_disease
|
HSCT: greater than or equal to 56 days from stem cell transplant with no evidence of active graft vs. host disease
| 3
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NCT02068612
|
8:21:treatment
|
Are on antipsychotic medications
| 3
|
[
"Are",
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[
0,
0,
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0
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NCT02690116
|
7:33:chronic_disease
|
Major severe clinical depression (fatigue-related factor)
| 3
|
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NCT02506192
|
9:17:chronic_disease
|
Treated Diabetes
| 3
|
[
"Treated",
"Diabetes"
] |
[
0,
2
] |
NCT02442102
|
39:52:chronic_disease,56:81:chronic_disease,89:95:chronic_disease,97:111:chronic_disease,113:124:chronic_disease
|
Presence of a central nervous system, neuromuscular or connective tissue disease (e.g., stroke, Guillain-Barre, scleroderma)
| 3
|
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NCT02422641
|
7:25:treatment,,,
|
Whole brain radiotherapy within the last 6 months or partial brain radiotherapy exceeding greater than 40% of total brain volume in the last 6 months
| 3
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NCT03113136
|
12:37:chronic_disease,
|
history of cardiac event or distress within the past 3 months
| 3
|
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NCT00967577
|
8:22:treatment,26:47:treatment,,66:75:treatment
|
Use of red blood cell or platelet transfusions within 4 weeks of treatment
| 3
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NCT01130077
|
8:26:treatment,
|
Use of immunosuppressives within four weeks prior to study entry
| 3
|
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NCT03181867
|
26:56:cancer
|
Histologically confirmed adenocarcinoma of the prostate
| 3
|
[
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[
0,
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NCT02578732
|
24:38:treatment,32:37:treatment,47:61:treatment
|
Patients with unstable biliary stents or with plastic stents. Information on type of stent is required at registration
| 3
|
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NCT02219555
|
1:23:chronic_disease
|
cervical radiculopathy
| 3
|
[
"cervical",
"radiculopathy"
] |
[
2,
2
] |
NCT02535832
|
1:8:treatment
|
Insulin resistant according to the Matsuda index
| 3
|
[
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NCT02525861
|
9:25:chronic_disease,31:54:chronic_disease,56:79:chronic_disease,81:104:chronic_disease,109:155:chronic_disease
|
Ongoing active infection with hepatitis A virus (HAV), hepatitis B virus (HBV), hepatitis C virus (HCV), or human immunodeficiency virus (HIV) Type 1 or 2 infection at the time of screening
| 3
|
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NCT02365090
|
,,33:39:chronic_disease,43:59:chronic_disease,,,117:131:chronic_disease
|
Prematurity ≥8 weeks Coexisting ocular or systemic disease Developmental delay Poor ocular alignment (strabismus >5 prism diopters)
| 3
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NCT01964859
|
7:24:chronic_disease
|
Known bleeding disorder
| 3
|
[
"Known",
"bleeding",
"disorder"
] |
[
0,
2,
2
] |
NCT02520713
|
36:54:treatment
|
Patients who have declined further anticancer therapy
| 3
|
[
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"anticancer",
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[
0,
0,
0,
0,
0,
1,
1
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NCT02843646
|
1:8:chronic_disease
|
Seizure history interfering with use of functional electrical stimulation as verified by their MD
| 3
|
[
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NCT01918644
|
9:42:cancer
|
treated non-melanoma/melanoma skin cancer
| 3
|
[
"treated",
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"skin",
"cancer"
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[
0,
3,
3,
3
] |
NCT02110069
|
123:131:chronic_disease,146:158:chronic_disease,178:197:chronic_disease,199:212:chronic_disease,216:229:chronic_disease,238:263:chronic_disease
|
Concurrent severe and/or uncontrolled medical disease that could compromise participation in the study (e.g. uncontrolled diabetes, uncontrolled hypertension, severe infection, severe malnutrition, chronic liver or renal disease, active upper GI tract ulceration)
| 3
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NCT00862433
|
1:18:chronic_disease,51:64:chronic_disease,66:83:chronic_disease,85:107:chronic_disease,109:122:chronic_disease,124:130:chronic_disease,132:159:chronic_disease
|
Organ malfunction, including (but not limited to) liver disease, pulmonary disease, ischemic heart disease, heart failure, stroke, peripheral vascular disease
| 3
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NCT02440581
|
62:77:chronic_disease,79:99:chronic_disease,101:111:chronic_disease
|
Clinical condition that may limit study participation (e.g., unstable angina, respiratory distress, infections)
| 3
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NCT02174016
|
12:27:chronic_disease
|
History of nephrolithiasis
| 3
|
[
"History",
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"nephrolithiasis"
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[
0,
0,
2
] |
NCT03040778
|
17:34:treatment
|
Patients taking CYP1A2 inhibitors
| 3
|
[
"Patients",
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[
0,
0,
1,
1
] |
NCT01893554
|
20:57:chronic_disease,98:101:chronic_disease,118:143:treatment,154:178:treatment,182:193:treatment,194:216:treatment
|
Known or suspected impairment of immunological functions, including maternal history of positive HIV test, receiving immunosuppressive therapy including systemic corticosteroids or bone marrow/solid organ transplant recipients
| 3
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NCT02352467
|
18:24:chronic_disease
|
Stage I pressure ulcers
| 3
|
[
"Stage",
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[
0,
0,
0,
2
] |
NCT02532595
|
1:16:chronic_disease
|
Fear of needles or unwilling to have needling performed due to fear or personal beliefs
| 3
|
[
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NCT01054196
|
102:114:allergy_name,126:137:allergy_name,142:151:allergy_name
|
History of allergic reactions attributed to compounds of similar chemical or biologic composition to lenalidomide (including thalidomide) or melphalan
| 3
|
[
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NCT02502006
|
1:21:cancer,25:45:cancer,58:66:treatment,71:102:cancer
|
cutaneous basal cell or squamous cell cancer resolved by excision, or carcinoma in situ of the cervix adequately treated
| 3
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NCT02562235
|
1:20:chronic_disease,,
|
Renal insufficiency (estimated glomerular filtration rate <30 mL/min/1.73m2 e.g. calculated based on Schwartz formula, for detailed calculation instructions
| 3
|
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0,
0,
0,
0,
0,
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0,
0,
0
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NCT01774019
|
1:29:chronic_disease
|
Biliary obstructive symptoms or signs
| 3
|
[
"Biliary",
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"symptoms",
"or",
"signs"
] |
[
2,
2,
2,
0,
0
] |
NCT00720785
|
1:38:chronic_disease
|
Psychiatric illness/social situations that would limit compliance with study requirements and ability to comprehend the investigational nature of the study and provide informed consent
| 3
|
[
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0,
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NCT01666080
|
70:77:chronic_disease
|
Occasionally donor derived engraftment may be present, but sustained aplasia or failed recovery of sufficient hematopoiesis requires administration of a second graft
| 3
|
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NCT00919503
|
15:41:chronic_disease,26:41:chronic_disease,46:60:chronic_disease,109:150:chronic_disease,154:188:chronic_disease
|
Patients with idiopathic aplastic anemia and Fanconi anemia; (patients with aplastic anemia associated with paroxysmal nocturnal hemoglobinuria [PNH] or inherited marrow failure syndromes, except Fanconi anemia, will be allowed)
| 3
|
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NCT02208362
|
45:57:cancer
|
Research participants with any other active malignancies
| 3
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NCT01760655
|
19:29:cancer,33:42:chronic_disease,122:126:treatment
|
Any hematological malignancy or dyscrasia not cited above which is thought to be high-risk with increased chance of post HSCT relapse
| 3
|
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NCT02963831
|
15:44:cancer,48:71:chronic_disease,144:159:treatment,163:178:treatment,
|
Subjects with asymptomatic brain metastases or spinal cord compression who have been treated, are considered stable, and who have not received corticosteroids or anticonvulsants for at least 28 days prior to screening may be included
| 3
|
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NCT02392572
|
,,,,,,,,,,,313:323:treatment
|
Women of child-bearing potential (i.e., women who are pre-menopausal or not surgically sterile) must use acceptable contraceptive methods (abstinence, intrauterine device [IUD], oral contraceptive or double barrier device, such as a condom, diaphragm, or cervical/vault cap), for 16 weeks after the last dose of study drug
| 3
|
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NCT02702492
|
1:20:treatment,
|
Palliative steroids for disease related symptoms < 7 days prior to C1D1
| 3
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NCT02424968
|
1:35:chronic_disease
|
Human immunodeficiency virus (HIV) positive
| 3
|
[
"Human",
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"(",
"HIV",
")",
"positive"
] |
[
2,
2,
2,
2,
0,
0,
0
] |
NCT02101944
|
,,140:158:treatment,
|
Patients must be able to avoid direct contact with pregnant or nursing women, infants and immunocompromised individuals during the days of reolysin treatment and for two days after
| 3
|
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NCT02133573
|
49:61:allergy_name,114:140:allergy_name,142:170:allergy_name,172:179:allergy_name,183:206:allergy_name,208:224:allergy_name,226:250:allergy_name,252:271:allergy_name,273:282:allergy_name
|
Known sensitivity or listed contraindication to progesterone (known allergy or hypersensitivity to progesterone, severe hepatic dysfunction, undiagnosed vaginal bleeding, mammary or genital tract carcinoma, thrombophlebitis, thromboembolic disorders, cerebral hemorrhage, porphyria)
| 3
|
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NCT02268253
|
,,,171:186:treatment
|
agrees to use acceptable contraceptive methods for the duration of time in the study, and to continue to use acceptable contraceptive methods for 2 months after the last SL-401 infusion
| 3
|
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NCT03176173
|
47:60:treatment,85:102:treatment,121:145:treatment,142:144:treatment,149:183:treatment,,304:320:cancer,322:360:treatment,356:359:treatment,
|
Has had restaging imaging after initiation of immunotherapy, at least 4 weeks after pre-immunotherapy baseline imaging; computed tomography (CT) or positron emission tomography (PET)/CT of at least chest/upper abdomen must be performed within 4 weeks prior to registration; for patients with history of brain metastases, brain magnetic resonance imaging (MRI) or CT is required within 4 weeks of registration; for other patients brain MRI or CT is required within 12 weeks of registration
| 3
|
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NCT02403193
|
12:34:treatment,
|
history of bilateral oophorectomy) or must have a negative serum pregnancy test upon study entry
| 3
|
[
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NCT02352467
|
1:6:chronic_disease
|
Ulcer of pressure/shear etiology (Stage II, III, and IV, see Appendix 9 for stage definitions)
| 3
|
[
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0
] |
NCT02725567
|
1:34:chronic_disease
|
Chronic kidney disease of Stage 3 or above
| 3
|
[
"Chronic",
"kidney",
"disease",
"of",
"Stage",
"3",
"or",
"above"
] |
[
2,
2,
2,
2,
2,
2,
0,
0
] |
NCT02058095
|
20:44:chronic_disease,,
|
Prior diagnosis of intrinsic renal diseases including renal artery stenosis of > 50%
| 3
|
[
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"diseases",
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"50",
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[
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2,
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0,
0,
0,
0,
0,
0
] |
NCT01872975
|
1:106:treatment,30:34:cancer,36:52:cancer
|
Patient must have clinically T1-3, N1 breast cancer at the time of diagnosis (before neoadjuvant therapy)
| 3
|
[
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",",
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NCT01434316
|
,,53:60:treatment,65:74:treatment,79:104:treatment,263:272:treatment
|
Pregnant women are excluded from this study because ABT-888 and SCH727965 are anti-proliferative agents with the potential for teratogenic or abortifacient effects; because there is an unknown but potential risk of adverse events in nursing infants secondary to treatment of the mother with ABT-888 and SCH727965, breastfeeding should be discontinued if the mother is treated with ABT-888 and SCH727965; these potential risks may also apply to other agents used in this study
| 3
|
[
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NCT02972840
|
26:29:cancer
|
Pathologically confirmed MCL, with documentation of a chromosome translocation t(11;14)(q13;q32) and/or overexpression of cyclin D1 in association with other relevant markers (eg, CD5, CD19, CD20, PAX5)
| 3
|
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NCT01773707
|
31:39:chronic_disease
|
Abnormal Glucose Tolerance or Diabetes
| 3
|
[
"Abnormal",
"Glucose",
"Tolerance",
"or",
"Diabetes"
] |
[
0,
0,
0,
0,
2
] |
NCT02203695
|
42:54:cancer,
|
Patients must be disease-free from prior malignancies for greater than 3 years
| 3
|
[
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"from",
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NCT02570672
|
33:51:chronic_disease,84:103:chronic_disease,105:133:chronic_disease,135:155:chronic_disease,157:185:chronic_disease,187:203:chronic_disease
|
Chronic inflammatory condition, autoimmune disease, or infectious processes (e.g., active tuberculosis, Human Immunodeficiency Virus, rheumatoid arthritis, systemic lupus erythematosus, hepatitis B or C)
| 3
|
[
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",",
"rheumatoid",
"arthritis",
",",
"systemic",
"lupus",
"erythematosus",
",",
"hepatitis",
"B",
"or",
"C",
")"
] |
[
0,
0,
0,
0,
2,
2,
0,
0,
0,
0,
0,
0,
0,
2,
2,
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2,
2,
2,
0,
2,
2,
0,
2,
2,
2,
0,
2,
2,
2,
2,
0
] |
NCT02451488
|
28:54:chronic_disease
|
Patients with a history of inflammatory bowel disease
| 3
|
[
"Patients",
"with",
"a",
"history",
"of",
"inflammatory",
"bowel",
"disease"
] |
[
0,
0,
0,
0,
0,
2,
2,
2
] |
NCT03062462
|
,,,104:120:treatment,
|
PAgR is more than 46% and the percentage of inhibition of ADP-induced platelet aggregation measured by thrombelastogram is not more than 30%
| 3
|
[
"PAgR",
"is",
"more",
"than",
"46",
"%",
"and",
"the",
"percentage",
"of",
"inhibition",
"of",
"ADP-induced",
"platelet",
"aggregation",
"measured",
"by",
"thrombelastogram",
"is",
"not",
"more",
"than",
"30",
"%"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
0,
0,
0,
0,
0
] |
NCT02601833
|
55:58:allergy_name
|
sensitivity to dental materials being used, including SDF
| 3
|
[
"sensitivity",
"to",
"dental",
"materials",
"being",
"used",
",",
"including",
"SDF"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
4
] |
NCT02498535
|
8:19:treatment,21:25:treatment,27:43:treatment,52:59:treatment,65:91:chronic_disease,
|
Use of antibiotics [oral, intravenous (iv), and/or inhaled] for acute respiratory symptoms within 2 weeks prior to baseline
| 3
|
[
"Use",
"of",
"antibiotics",
"[",
"oral",
",",
"intravenous",
"(",
"iv",
")",
",",
"and/or",
"inhaled",
"]",
"for",
"acute",
"respiratory",
"symptoms",
"within",
"2",
"weeks",
"prior",
"to",
"baseline"
] |
[
0,
0,
1,
0,
1,
0,
1,
1,
0,
0,
0,
0,
1,
0,
0,
2,
2,
2,
0,
0,
0,
0,
0,
0
] |
NCT02562755
|
1:52:chronic_disease
|
Adequate hematological, hepatic, and renal function
| 3
|
[
"Adequate",
"hematological",
",",
"hepatic",
",",
"and",
"renal",
"function"
] |
[
2,
2,
2,
2,
2,
2,
0,
0
] |
NCT01306019
|
1:21:cancer,,
|
Childhood malignancy (occurring before 18 years of age) in the patient or a first degree relative
| 3
|
[
"Childhood",
"malignancy",
"(",
"occurring",
"before",
"18",
"years",
"of",
"age",
")",
"in",
"the",
"patient",
"or",
"a",
"first",
"degree",
"relative"
] |
[
3,
3,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT01174121
|
12:36:chronic_disease
|
Concurrent opportunistic infections
| 3
|
[
"Concurrent",
"opportunistic",
"infections"
] |
[
0,
2,
2
] |
NCT03089281
|
26:59:treatment
|
have previously received cardiac resynchronization therapy with pacing in the left ventricle
| 3
|
[
"have",
"previously",
"received",
"cardiac",
"resynchronization",
"therapy",
"with",
"pacing",
"in",
"the",
"left",
"ventricle"
] |
[
0,
0,
0,
1,
1,
1,
0,
0,
0,
0,
0,
0
] |
NCT01734512
|
53:56:treatment
|
Progressive or recurrent disease should be based on MRI according to the definition below
| 3
|
[
"Progressive",
"or",
"recurrent",
"disease",
"should",
"be",
"based",
"on",
"MRI",
"according",
"to",
"the",
"definition",
"below"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
0,
0,
0,
0
] |
NCT02227199
|
22:63:treatment,
|
Patients must have a CT of chest, abdomen, and pelvis with PET within 28 days of enrollment
| 3
|
[
"Patients",
"must",
"have",
"a",
"CT",
"of",
"chest",
",",
"abdomen",
",",
"and",
"pelvis",
"with",
"PET",
"within",
"28",
"days",
"of",
"enrollment"
] |
[
0,
0,
0,
0,
1,
1,
1,
1,
1,
1,
1,
1,
0,
0,
0,
0,
0,
0,
0
] |
NCT02413047
|
5:44:chronic_disease,46:55:chronic_disease,57:64:chronic_disease,66:71:chronic_disease,73:92:chronic_disease,103:119:chronic_disease
|
Any unstable or uncontrolled cardiovascular, pulmonary, hepatic, renal, endocrine/metabolic, or other medical disorder that, in the opinion of the investigator, would confound the study results or compromise patient safety
| 3
|
[
"Any",
"unstable",
"or",
"uncontrolled",
"cardiovascular",
",",
"pulmonary",
",",
"hepatic",
",",
"renal",
",",
"endocrine/metabolic",
",",
"or",
"other",
"medical",
"disorder",
"that",
",",
"in",
"the",
"opinion",
"of",
"the",
"investigator",
",",
"would",
"confound",
"the",
"study",
"results",
"or",
"compromise",
"patient",
"safety"
] |
[
0,
2,
2,
2,
2,
0,
2,
0,
2,
0,
2,
0,
2,
0,
0,
0,
2,
2,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02283333
|
21:45:chronic_disease
|
with a diagnosis of Prolonged Grief Disorder
| 3
|
[
"with",
"a",
"diagnosis",
"of",
"Prolonged",
"Grief",
"Disorder"
] |
[
0,
0,
0,
0,
2,
2,
2
] |
NCT02102854
|
40:67:treatment
|
Rejection episode requiring the use of therapeutic plasma exchange immediately subsequent to rATG administration
| 3
|
[
"Rejection",
"episode",
"requiring",
"the",
"use",
"of",
"therapeutic",
"plasma",
"exchange",
"immediately",
"subsequent",
"to",
"rATG",
"administration"
] |
[
0,
0,
0,
0,
0,
0,
1,
1,
1,
0,
0,
0,
0,
0
] |
NCT02578901
|
26:48:cancer,52:59:chronic_disease
|
Confirmed diagnosis of a hematologic malignancy or aplasia
| 3
|
[
"Confirmed",
"diagnosis",
"of",
"a",
"hematologic",
"malignancy",
"or",
"aplasia"
] |
[
0,
0,
0,
0,
3,
3,
0,
2
] |
NCT01508390
|
17:43:chronic_disease
|
No diagnosis of inflammatory bowel disease
| 3
|
[
"No",
"diagnosis",
"of",
"inflammatory",
"bowel",
"disease"
] |
[
0,
0,
0,
2,
2,
2
] |
NCT02512926
|
71:89:treatment,91:104:treatment,106:118:treatment,123:130:treatment
|
Patient must have fully recovered from the acute toxic effects of all prior chemotherapy, immunotherapy, radiotherapy, or surgery prior to study entry
| 3
|
[
"Patient",
"must",
"have",
"fully",
"recovered",
"from",
"the",
"acute",
"toxic",
"effects",
"of",
"all",
"prior",
"chemotherapy",
",",
"immunotherapy",
",",
"radiotherapy",
",",
"or",
"surgery",
"prior",
"to",
"study",
"entry"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1,
0,
1,
0,
1,
0,
0,
1,
0,
0,
0,
0
] |
NCT02236000
|
1:27:chronic_disease
|
inflammatory bowel disease
| 3
|
[
"inflammatory",
"bowel",
"disease"
] |
[
2,
2,
2
] |
NCT02301611
|
1:26:chronic_disease,47:50:chronic_disease,52:55:chronic_disease,57:60:chronic_disease
|
Immune deficiency disease or known history of HIV, HBV, HCV
| 3
|
[
"Immune",
"deficiency",
"disease",
"or",
"known",
"history",
"of",
"HIV",
",",
"HBV",
",",
"HCV"
] |
[
2,
2,
2,
0,
0,
0,
0,
2,
0,
2,
0,
2
] |
NCT01824836
|
12:34:treatment
|
history of bilateral oophorectomy
| 3
|
[
"history",
"of",
"bilateral",
"oophorectomy"
] |
[
0,
0,
1,
1
] |
NCT02369458
|
104:115:allergy_name
|
A history of allergic reactions attributed to compounds of similar chemical or biologic composition to mitomycin C or other agents used in the study
| 3
|
[
"A",
"history",
"of",
"allergic",
"reactions",
"attributed",
"to",
"compounds",
"of",
"similar",
"chemical",
"or",
"biologic",
"composition",
"to",
"mitomycin",
"C",
"or",
"other",
"agents",
"used",
"in",
"the",
"study"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
4,
4,
0,
0,
0,
0,
0,
0,
0
] |
NCT01794793
|
,,,,183:192:treatment,,233:249:treatment,,286:301:treatment
|
Women of child-bearing potential, defined as all women physiologically capable of becoming pregnant, unless they are using highly effective methods of contraception during the study treatment and for 30 days after the final dose of pasireotide s.c. and 84 days after the final dose of pasireotide LAR
| 3
|
[
"Women",
"of",
"child-bearing",
"potential",
",",
"defined",
"as",
"all",
"women",
"physiologically",
"capable",
"of",
"becoming",
"pregnant",
",",
"unless",
"they",
"are",
"using",
"highly",
"effective",
"methods",
"of",
"contraception",
"during",
"the",
"study",
"treatment",
"and",
"for",
"30",
"days",
"after",
"the",
"final",
"dose",
"of",
"pasireotide",
"s.c.",
"and",
"84",
"days",
"after",
"the",
"final",
"dose",
"of",
"pasireotide",
"LAR"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02425904
|
,,106:109:chronic_disease
|
AST (SGOT)/ALT (SGPT) < 2.5 X institutional upper limit of normal unless it is related to involvement by LCH
| 3
|
[
"AST",
"(",
"SGOT",
")",
"/ALT",
"(",
"SGPT",
")",
"<",
"2.5",
"X",
"institutional",
"upper",
"limit",
"of",
"normal",
"unless",
"it",
"is",
"related",
"to",
"involvement",
"by",
"LCH"
] |
[
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
2
] |
NCT02515110
|
36:68:cancer
|
patients with margins positive for lobular carcinoma in situ (LCIS) are eligible without additional resection
| 3
|
[
"patients",
"with",
"margins",
"positive",
"for",
"lobular",
"carcinoma",
"in",
"situ",
"(",
"LCIS",
")",
"are",
"eligible",
"without",
"additional",
"resection"
] |
[
0,
0,
0,
0,
0,
3,
3,
3,
3,
3,
0,
0,
0,
0,
0,
0,
0
] |
NCT02551679
|
20:37:treatment,
|
Subject received a blood transfusion during the previous 4 weeks (to exclude the potential of non-autologous ACPs in the harvested blood)
| 3
|
[
"Subject",
"received",
"a",
"blood",
"transfusion",
"during",
"the",
"previous",
"4",
"weeks",
"(",
"to",
"exclude",
"the",
"potential",
"of",
"non-autologous",
"ACPs",
"in",
"the",
"harvested",
"blood",
")"
] |
[
0,
0,
0,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT01988246
|
1:10:treatment,16:27:treatment,31:50:treatment,,93:100:treatment
|
Treatment with intraocular or periocular steroids in the study eye within 3 months prior to surgery
| 3
|
[
"Treatment",
"with",
"intraocular",
"or",
"periocular",
"steroids",
"in",
"the",
"study",
"eye",
"within",
"3",
"months",
"prior",
"to",
"surgery"
] |
[
1,
0,
1,
0,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1
] |
NCT02448173
|
,29:59:cancer
|
Patients with more than one malignant primary colon cancer will be excluded
| 3
|
[
"Patients",
"with",
"more",
"than",
"one",
"malignant",
"primary",
"colon",
"cancer",
"will",
"be",
"excluded"
] |
[
0,
0,
0,
0,
0,
3,
3,
3,
3,
0,
0,
0
] |
NCT02073097
|
,5:21:cancer
|
≥ 2 extranodal sites (1 point)
| 3
|
[
"≥",
"2",
"extranodal",
"sites",
"(",
"1",
"point",
")"
] |
[
0,
0,
3,
3,
0,
0,
0,
0
] |
NCT01367444
|
5:45:treatment,
|
Any periocular injections of corticosteroids to the treated eye within 4 months prior to screening
| 3
|
[
"Any",
"periocular",
"injections",
"of",
"corticosteroids",
"to",
"the",
"treated",
"eye",
"within",
"4",
"months",
"prior",
"to",
"screening"
] |
[
0,
1,
1,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02481245
|
12:38:chronic_disease
|
History of Type 1 or Type II Diabetes
| 3
|
[
"History",
"of",
"Type",
"1",
"or",
"Type",
"II",
"Diabetes"
] |
[
0,
0,
2,
2,
2,
2,
2,
2
] |
NCT02312570
|
10:19:treatment,21:30:treatment,34:43:treatment,
|
Received allograft, autograft or xenograft within 30 days of enrollment
| 3
|
[
"Received",
"allograft",
",",
"autograft",
"or",
"xenograft",
"within",
"30",
"days",
"of",
"enrollment"
] |
[
0,
1,
0,
1,
0,
1,
0,
0,
0,
0,
0
] |
NCT02982772
|
29:45:allergy_name
|
History of allergies to the nicotine patches
| 3
|
[
"History",
"of",
"allergies",
"to",
"the",
"nicotine",
"patches"
] |
[
0,
0,
0,
0,
0,
4,
4
] |
NCT03093272
|
1:17:chronic_disease,25:59:chronic_disease,63:78:chronic_disease
|
Active infection (e.g., human immunodeficiency virus [HIV] or viral hepatitis)
| 3
|
[
"Active",
"infection",
"(",
"e.g.",
",",
"human",
"immunodeficiency",
"virus",
"[",
"HIV",
"]",
"or",
"viral",
"hepatitis",
")"
] |
[
2,
2,
0,
0,
0,
2,
2,
2,
2,
0,
0,
0,
2,
2,
0
] |
NCT02373644
|
1:17:treatment,21:43:treatment,
|
Physical therapy or chiropractic treatment for low back pain in the 3 months before initial examination
| 3
|
[
"Physical",
"therapy",
"or",
"chiropractic",
"treatment",
"for",
"low",
"back",
"pain",
"in",
"the",
"3",
"months",
"before",
"initial",
"examination"
] |
[
1,
1,
0,
1,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT02252432
|
25:33:treatment,37:46:treatment,47:63:treatment
|
Those already receiving ketamine or methadone prior to surgery
| 3
|
[
"Those",
"already",
"receiving",
"ketamine",
"or",
"methadone",
"prior",
"to",
"surgery"
] |
[
0,
0,
0,
1,
0,
1,
1,
1,
1
] |
NCT01880567
|
17:20:cancer,,
|
Newly diagnosed MCL: Age > 65 years at the time of signing the informed consent
| 3
|
[
"Newly",
"diagnosed",
"MCL",
":",
"Age",
">",
"65",
"years",
"at",
"the",
"time",
"of",
"signing",
"the",
"informed",
"consent"
] |
[
0,
0,
3,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0
] |
NCT03145181
|
31:46:treatment,,113:123:treatment,,203:226:treatment
|
Received a cumulative dose of corticosteroids equivalent to greater than or equal to (>=) 140 milligram (mg) of prednisone within the 14-day period before the first dose of study drug (does not include pretreatment medication)
| 3
|
[
"Received",
"a",
"cumulative",
"dose",
"of",
"corticosteroids",
"equivalent",
"to",
"greater",
"than",
"or",
"equal",
"to",
"(",
">",
"=",
")",
"140",
"milligram",
"(",
"mg",
")",
"of",
"prednisone",
"within",
"the",
"14-day",
"period",
"before",
"the",
"first",
"dose",
"of",
"study",
"drug",
"(",
"does",
"not",
"include",
"pretreatment",
"medication",
")"
] |
[
0,
0,
0,
0,
0,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
0,
1,
1,
0
] |
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