Datasets:
SKT27182
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NER_processed_data

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NCT02851407
,,,,206:217:treatment,
Female patients (and female partners of male patients) of childbearing potential who are sexually active must agree to use a highly effective method of contraception with their partners during exposure to defibrotide and for 1 week after the last dose of defibrotide
1
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NCT02911116
1:15:chronic_disease
Active disease is defined
1
[ "Active", "disease", "is", "defined" ]
[ 2, 2, 0, 0 ]
NCT02925923
1:12:treatment
Rivaroxaban
1
[ "Rivaroxaban" ]
[ 1 ]
NCT02360579
,,54:76:chronic_disease,78:88:chronic_disease,130:153:chronic_disease
Patients ≥ 60 years of age and who have a history of ischemic heart disease, chest pain, or clinically significant atrial and/or ventricular arrhythmias must have a cardiac stress test. Patients with any irreversible wall movement abnormalities
1
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NCT01059786
13:24:chronic_disease
Presence of CNS disease
1
[ "Presence", "of", "CNS", "disease" ]
[ 0, 0, 2, 2 ]
NCT01915095
71:81:treatment
Able to perform some small wrist flexion and extension (measured by a goniometer)
1
[ "Able", "to", "perform", "some", "small", "wrist", "flexion", "and", "extension", "(", "measured", "by", "a", "goniometer", ")" ]
[ 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 1, 0 ]
NCT01061515
21:33:treatment
have received prior chemotherapy
1
[ "have", "received", "prior", "chemotherapy" ]
[ 0, 0, 0, 1 ]
NCT02592551
106:115:treatment
Any condition that, in the opinion of the investigator, would interfere with the evaluation of the study treatment or interpretation of subject safety or study results
1
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NCT02525692
20:39:treatment,51:60:treatment,,118:128:treatment
Concomitant use of CYP3A4/5 inhibitors during the treatment phase of the study and within 72 hours prior to starting study drug administration
1
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[ 0, 0, 0, 1, 1, 0, 0, 1, 0, 0, 0, 1, 1, 0, 0, 0, 0, 0, 0, 0, 0, 0 ]
NCT03102320
1:34:chronic_disease
Active hepatitis B or C infection
1
[ "Active", "hepatitis", "B", "or", "C", "infection" ]
[ 2, 2, 2, 2, 2, 2 ]
NCT00738101
24:45:treatment,
Be expected to require intravenous nutrition for at least an additional 28 days
1
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[ 0, 0, 0, 0, 1, 1, 0, 0, 0, 0, 0, 0, 0 ]
NCT02411656
34:62:cancer,92:95:cancer,180:188:chronic_disease,193:198:chronic_disease,200:213:chronic_disease,335:360:cancer,414:440:cancer,546:578:cancer,,
Has histological confirmation of HER2 normal breast carcinoma with a clinical diagnosis of IBC based on presence of inflammatory changes in the involved breast, including diffuse erythema and edema (peau d'orange), with or without an underlying palpable mass involving the majority of the skin of the breast; pathological evidence of dermal lymphatic invasion should be noted but is not required for diagnosis of inflammatory breast cancer regardless estrogen receptor (ER)/progesterone receptor (PR) status; OR has histological confirmation of triple negative breast carcinoma (HER2 normal, ER/PR < 10%) without clinical diagnosis of IBC
1
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NCT03085784
18:45:treatment,62:86:cancer,122:143:chronic_disease
Undergone either ocular or orbital radiation for any primary ocular or orbital cancer within clinical evidence of having radiation retinopathy
1
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[ 0, 0, 3, 3, 3, 2, 2, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0 ]
NCT02140255
11:14:chronic_disease
No plasma HIV RNA detected at Step 2 Week 48 and thereafter
1
[ "No", "plasma", "HIV", "RNA", "detected", "at", "Step", "2", "Week", "48", "and", "thereafter" ]
[ 0, 0, 2, 0, 0, 0, 0, 0, 0, 0, 0, 0 ]
NCT02229565
15:37:treatment,79:88:treatment,92:97:treatment,101:114:treatment
Patients with prior systemic therapy will not be eligible for the study, i.e. radiation or chemo or immunotherapy
1
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[ 0, 0, 1, 1, 1, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 1, 0, 1, 0, 1 ]
NCT02423863
1:8:cancer,,
Sarcoma Patients must be 14 years of age or older
1
[ "Sarcoma", "Patients", "must", "be", "14", "years", "of", "age", "or", "older" ]
[ 3, 0, 0, 0, 0, 0, 0, 0, 0, 0 ]
NCT02094794
32:42:treatment
the patient, family member and transplant staff physician (physician, nurse, and social worker) meet at least once prior to starting the transplant procedure
1
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NCT02400255
1:16:treatment,,,76:94:treatment,105:120:treatment,
Post-transplant bone marrow blast count ≤ 5% confirmed by standard of care bone marrow biopsy performed post-transplant (at least 30 days post-transplant)
1
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NCT02875405
1:16:chronic_disease
chest deformity
1
[ "chest", "deformity" ]
[ 2, 2 ]
NCT02718001
15:33:treatment
High risk for open-heart surgery
1
[ "High", "risk", "for", "open-heart", "surgery" ]
[ 0, 0, 0, 1, 1 ]
NCT03070899
,49:58:treatment
planning a pregnancy within the duration of the treatment period of the study
1
[ "planning", "a", "pregnancy", "within", "the", "duration", "of", "the", "treatment", "period", "of", "the", "study" ]
[ 0, 0, 0, 0, 0, 0, 0, 0, 1, 0, 0, 0, 0 ]
NCT02271919
19:39:treatment,47:69:treatment,73:96:treatment,141:151:treatment,
Plan to use other nicotine substitutes (i.e., over-the-counter [OTC] or prescription medication for smoking cessation) or smoking cessation treatments in the next 12 months
1
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NCT02525692
102:108:treatment
History of allergic reactions attributed to compounds of similar chemical or biologic composition to ONC201 or its excipients
1
[ "History", "of", "allergic", "reactions", "attributed", "to", "compounds", "of", "similar", "chemical", "or", "biologic", "composition", "to", "ONC201", "or", "its", "excipients" ]
[ 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 1, 0, 0, 0 ]
NCT02412540
16:25:treatment,
Stable dose of vitamin E that was started 12 months or more prior to biopsy is allowed
1
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[ 0, 0, 0, 1, 1, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0 ]
NCT03082612
46:58:treatment
Treatment plans to include weekly outpatient chemotherapy
1
[ "Treatment", "plans", "to", "include", "weekly", "outpatient", "chemotherapy" ]
[ 0, 0, 0, 0, 0, 0, 1 ]
NCT02564744
122:130:cancer
Participants must have evaluable or measurable disease in accordance with the International Working Group Guidelines for Lymphoma
1
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NCT02151175
17:50:chronic_disease
Subjects with a cognitive or psychiatric disorder that limits the ability to give informed consent or are unable to cooperate with the testing
1
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NCT02069925
10:25:chronic_disease
Unstable medical illness
1
[ "Unstable", "medical", "illness" ]
[ 0, 2, 2 ]
NCT02553642
,32:42:treatment,47:56:treatment,58:83:treatment,88:112:treatment
Must be at least 28 days since craniotomy and resection, stereotactic radiosurgery, or whole brain radiotherapy
1
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NCT02188745
62:68:treatment,73:81:treatment,86:95:treatment
Baseline radiographic staging, including specifically either PET/CT, or CT (CAP) and bone scan
1
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NCT02422641
,,,67:83:cancer
Alkaline phosphatase <2.5x the ULN or <5x the ULN if secondary to liver metastasis
1
[ "Alkaline", "phosphatase", "<", "2.5x", "the", "ULN", "or", "<", "5x", "the", "ULN", "if", "secondary", "to", "liver", "metastasis" ]
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NCT02159027
9:19:cancer
Current malignancy
1
[ "Current", "malignancy" ]
[ 0, 3 ]
NCT01893554
23:34:treatment,43:66:treatment,84:107:chronic_disease,109:118:treatment,124:143:treatment,155:171:treatment,173:192:treatment,198:223:treatment
Permitted concomitant medications include nutritional supplements, medications for gastroesophageal reflux, eye drops, and topical medications, including topical steroids, topical antibiotics, and topical antifungal agents
1
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NCT02594111
1:13:treatment
ketoconazole
1
[ "ketoconazole" ]
[ 1 ]
NCT02477826
45:63:chronic_disease
Subjects with an active, known or suspected autoimmune disease
1
[ "Subjects", "with", "an", "active", ",", "known", "or", "suspected", "autoimmune", "disease" ]
[ 0, 0, 0, 0, 0, 0, 0, 0, 2, 2 ]
NCT03059030
50:80:cancer
worsens postoperative survival in the setting of hepatocellular carcinoma (HCC)
1
[ "worsens", "postoperative", "survival", "in", "the", "setting", "of", "hepatocellular", "carcinoma", "(", "HCC", ")" ]
[ 0, 0, 0, 0, 0, 0, 0, 3, 3, 3, 0, 0 ]
NCT02613936
12:21:chronic_disease
history of psychosis
1
[ "history", "of", "psychosis" ]
[ 0, 0, 2 ]
NCT02911792
1:27:chronic_disease
major organ system disease
1
[ "major", "organ", "system", "disease" ]
[ 2, 2, 2, 2 ]
NCT02393794
1:25:chronic_disease,,
ncontrolled hypertension, i.e., blood pressure (BP) of ≥ 160/95
1
[ "ncontrolled", "hypertension", ",", "i.e.", ",", "blood", "pressure", "(", "BP", ")", "of", "≥", "160/95" ]
[ 2, 2, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0 ]
NCT02277548
33:50:treatment
Patients anticipated to receive radiation therapy with Protons
1
[ "Patients", "anticipated", "to", "receive", "radiation", "therapy", "with", "Protons" ]
[ 0, 0, 0, 0, 1, 1, 0, 0 ]
NCT02508038
57:76:treatment
Is free from communicable disease risks associated with xenotransplantation
1
[ "Is", "free", "from", "communicable", "disease", "risks", "associated", "with", "xenotransplantation" ]
[ 0, 0, 0, 0, 0, 0, 0, 0, 1 ]
NCT01822522
,,,100:109:treatment
Hemoptysis of >= 0.5 teaspoon (2.5 mL) of red blood within 3 months before the first dose of study treatment
1
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[ 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 1 ]
NCT02035085
1:11:treatment,16:33:treatment,38:54:cancer
Lumpectomy and radiation therapy for breast carcinoma
1
[ "Lumpectomy", "and", "radiation", "therapy", "for", "breast", "carcinoma" ]
[ 1, 0, 1, 1, 0, 3, 3 ]
NCT02184520
1:16:chronic_disease
pseudoarthrosis (failed previous fusion)
1
[ "pseudoarthrosis", "(", "failed", "previous", "fusion", ")" ]
[ 2, 0, 0, 0, 0, 0 ]
NCT01495637
16:33:treatment
Presence of an endotracheal tube at the time of enrollment
1
[ "Presence", "of", "an", "endotracheal", "tube", "at", "the", "time", "of", "enrollment" ]
[ 0, 0, 0, 1, 1, 0, 0, 0, 0, 0 ]
NCT02467478
16:20:treatment,24:59:treatment,71:80:treatment,85:92:treatment
Current use of oral or injectable anti-diabetic medication other than Metformin and insulin
1
[ "Current", "use", "of", "oral", "or", "injectable", "anti-diabetic", "medication", "other", "than", "Metformin", "and", "insulin" ]
[ 0, 0, 0, 1, 0, 1, 1, 1, 0, 0, 1, 0, 1 ]
NCT01859819
50:58:cancer
Patients with newly diagnosed Group A (low risk) lymphoma
1
[ "Patients", "with", "newly", "diagnosed", "Group", "A", "(", "low", "risk", ")", "lymphoma" ]
[ 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 3 ]
NCT02131389
15:38:treatment,51:55:treatment,57:89:treatment
Has undergone partial hip replacement or previous ORIF (open reduction internal fixation of femur or acetabulum)
1
[ "Has", "undergone", "partial", "hip", "replacement", "or", "previous", "ORIF", "(", "open", "reduction", "internal", "fixation", "of", "femur", "or", "acetabulum", ")" ]
[ 0, 0, 1, 1, 1, 0, 0, 1, 0, 1, 1, 1, 1, 0, 0, 0, 0, 0 ]
NCT03115424
14:41:treatment,
Prior use of glucose lowering medication in the 3 months prior to screening
1
[ "Prior", "use", "of", "glucose", "lowering", "medication", "in", "the", "3", "months", "prior", "to", "screening" ]
[ 0, 0, 0, 1, 1, 1, 0, 0, 0, 0, 0, 0, 0 ]
NCT00716066
1:14:chronic_disease,,,,
Renal disease with estimated glomerular filtration rate (GFR) by creatinine clearance or iothalamate clearance < 50 ml/min/1.73 m^2 body surface area
1
[ "Renal", "disease", "with", "estimated", "glomerular", "filtration", "rate", "(", "GFR", ")", "by", "creatinine", "clearance", "or", "iothalamate", "clearance", "<", "50", "ml/min/1.73", "m^2", "body", "surface", "area" ]
[ 2, 2, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0 ]
NCT01896999
46:58:treatment
Patients must have relapsed after first line chemotherapy
1
[ "Patients", "must", "have", "relapsed", "after", "first", "line", "chemotherapy" ]
[ 0, 0, 0, 0, 0, 0, 0, 1 ]
NCT02445768
9:21:chronic_disease
another brain injury or illness related to the brain that has lasting effects or effects experienced at the moment of recruitment
1
[ "another", "brain", "injury", "or", "illness", "related", "to", "the", "brain", "that", "has", "lasting", "effects", "or", "effects", "experienced", "at", "the", "moment", "of", "recruitment" ]
[ 0, 2, 2, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0 ]
NCT02518594
20:44:treatment,,
Cervical length on transvaginal examination of less than 30 mm within 10 days prior to randomization by a study certified sonographer
1
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[ 0, 0, 0, 1, 1, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0 ]
NCT02332850
1:19:treatment,23:43:cancer,47:82:cancer,87:105:cancer,95:105:cancer,116:131:cancer,138:154:treatment
complete resection of basal cell carcinoma or squamous cell carcinoma of the skin, an in situ malignancy, low-risk prostate cancer after curative therapy or complete resection of other advanced malignancy with the expectation that the patient has received curative therapy
1
[ "complete", "resection", "of", "basal", "cell", "carcinoma", "or", "squamous", "cell", "carcinoma", "of", "the", "skin", ",", "an", "in", "situ", "malignancy", ",", "low-risk", "prostate", "cancer", "after", "curative", "therapy", "or", "complete", "resection", "of", "other", "advanced", "malignancy", "with", "the", "expectation", "that", "the", "patient", "has", "received", "curative", "therapy" ]
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NCT02547662
13:20:chronic_disease,24:43:chronic_disease,132:141:treatment
Any serious medical or psychiatric illness that could, in the investigator's opinion, potentially interfere with the completion of treatment according to this protocol
1
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NCT02311621
1:20:cancer
Skull based disease with soft tissue extension
1
[ "Skull", "based", "disease", "with", "soft", "tissue", "extension" ]
[ 3, 3, 3, 0, 0, 0, 0 ]
NCT02746458
,156:175:treatment
Injuries to other body systems (or other medical conditions) that would preclude the ability to weight bear as tolerated and initiate PT within 28 days of definitive fixation
1
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NCT01896999
32:48:treatment
patients may not have received prior ipilimumab
1
[ "patients", "may", "not", "have", "received", "prior", "ipilimumab" ]
[ 0, 0, 0, 0, 0, 1, 1 ]
NCT01341080
33:55:chronic_disease
Subjects will be diagnosed with Parkinson Disease (PD) by the UK Brain Bank criteria
1
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NCT02920086
1:19:chronic_disease,11:19:chronic_disease,132:145:chronic_disease
End-stage dementia (inability to perform all ADLs, mutism or minimal verbal output secondary to dementia, bed-bound state prior to acute illness)
1
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NCT02383927
,,27:51:chronic_disease
NYHA Grade III or greater congestive heart failure
1
[ "NYHA", "Grade", "III", "or", "greater", "congestive", "heart", "failure" ]
[ 0, 0, 0, 0, 0, 2, 2, 2 ]
NCT02809677
11:43:chronic_disease,67:93:chronic_disease,100:124:chronic_disease,126:141:chronic_disease,143:170:chronic_disease,175:181:cancer,222:228:chronic_disease,230:237:chronic_disease,239:249:chronic_disease
severe or life-threatening medical illness, such as other serious cardiopulmonary conditions (e.g. congenital heart disease, cystic fibrosis, alpha-1-antitrypsin disease) or cancer, which would confound the assessment of asthma, anxiety, depression or quality of life
1
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NCT01622868
7:26:cancer,35:63:cancer,85:112:cancer,144:151:cancer,167:180:cancer,
Prior invasive malignancy (except non-melanomatous skin cancer, curatively resected thyroid papillary carcinoma, and invasive and non-invasive cancers related to the breast cancer) unless disease free for a minimum of 3 years
1
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NCT02315612
1:21:treatment,39:58:treatment,60:74:treatment
immunohistochemistry will be used for lymph node biopsies, flow cytometry will be used for peripheral blood and bone marrow samples and CSF when feasible
1
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NCT03042767
1:14:chronic_disease,,,
Acute illness within past 2 weeks prior to enrollment (defined as fever > 100.4ºF)
1
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NCT01896999
,,114:128:treatment
a female of childbearing potential is any woman, regardless of sexual orientation or whether they have undergone tubal ligation
1
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NCT02008656
4:21:chronic_disease,32:61:treatment,63:79:treatment
No active infections requiring systemic antibiotic treatment (oral antibiotics are acceptable at the discretion of the treating physician)
1
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[ 0, 2, 2, 0, 1, 1, 1, 0, 1, 1, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0 ]
NCT00540761
13:46:chronic_disease
unprotected left main coronary artery disease
1
[ "unprotected", "left", "main", "coronary", "artery", "disease" ]
[ 0, 2, 2, 2, 2, 2 ]
NCT01829958
1:16:chronic_disease,18:33:chronic_disease,37:55:chronic_disease
Serous effusion (plural effusion or peritoneal ascites)
1
[ "Serous", "effusion", "(", "plural", "effusion", "or", "peritoneal", "ascites", ")" ]
[ 2, 2, 0, 2, 2, 0, 2, 2, 0 ]
NCT02370693
33:43:allergy_name,45:50:allergy_name,54:62:allergy_name
Patient has hypersensitivity to bortezomib, boron or mannitol
1
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NCT03036280
1:22:chronic_disease,42:56:chronic_disease,58:74:chronic_disease,76:85:chronic_disease
Psychiatric diagnosis or symptoms (e.g., hallucinations, major depression, delusions, etc.)
1
[ "Psychiatric", "diagnosis", "or", "symptoms", "(", "e.g.", ",", "hallucinations", ",", "major", "depression", ",", "delusions", ",", "etc", ".", ")" ]
[ 2, 2, 0, 0, 0, 0, 0, 2, 0, 2, 2, 0, 2, 0, 0, 0, 0 ]
NCT02536794
38:56:chronic_disease
Patients with a history of or active autoimmune disease
1
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[ 0, 0, 0, 0, 0, 0, 0, 2, 2 ]
NCT02488967
27:40:cancer
By pathologic evaluation, primary tumor must be pT1-3
1
[ "By", "pathologic", "evaluation", ",", "primary", "tumor", "must", "be", "pT1-3" ]
[ 0, 0, 0, 0, 3, 3, 0, 0, 0 ]
NCT02479620
1:14:chronic_disease
osteomyelitis of the metatarsal or more proximal region
1
[ "osteomyelitis", "of", "the", "metatarsal", "or", "more", "proximal", "region" ]
[ 2, 0, 0, 0, 0, 0, 0, 0 ]
NCT01880567
16:27:chronic_disease
positive serum hepatitis B antibody
1
[ "positive", "serum", "hepatitis", "B", "antibody" ]
[ 0, 0, 2, 2, 0 ]
NCT02520791
43:61:chronic_disease
Patients with active, known, or suspected autoimmune disease
1
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[ 0, 0, 0, 0, 0, 0, 0, 0, 2, 2 ]
NCT02251431
1:24:treatment
Prior bariatric surgery
1
[ "Prior", "bariatric", "surgery" ]
[ 1, 1, 1 ]
NCT02479698
12:34:treatment
history of solid organ transplant
1
[ "history", "of", "solid", "organ", "transplant" ]
[ 0, 0, 1, 1, 1 ]
NCT01585402
33:37:chronic_disease
Subjects must be diagnosed with ACDC based on genetic tests confirming mutation(s) in NT5E and evidence of lower extremity arterial calcifications
1
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NCT02975986
22:27:treatment,25:27:treatment,,58:79:chronic_disease,,,107:118:treatment,120:150:treatment,170:186:chronic_disease,203:216:chronic_disease,,,,,368:374:chronic_disease,380:447:treatment,456:480:treatment
Contraindications to SPECT/CT, pregnancy, breastfeeding, chronic renal disease (eGFR < 60 ml/min/1.73m2), proteinuria, genetic diseases of the kidney, inborn defects of lipid metabolism, alcohol abuse, liver disease (patients with highly elevated total bilirubin, elevated liver enzymes AST, ALT and alkaline phosphatase and those with an established liver disease), anemia, and pharmacological treatment with insulin or insulin-sensitizing drugs such as thiazolidinediones (TZD)
1
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NCT01871766
,,,,,,143:152:treatment
Female participants ≥ 10 years of age or post-menarchal must have a negative serum or urine pregnancy test within 24 hours prior to beginning treatment
1
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NCT02508038
8:46:chronic_disease
active Central Nervous System (CNS) infection
1
[ "active", "Central", "Nervous", "System", "(", "CNS", ")", "infection" ]
[ 0, 2, 2, 2, 2, 2, 0, 0 ]
NCT01970306
47:64:allergy_name
Patients with known sensitivity or allergy to porcine materials
1
[ "Patients", "with", "known", "sensitivity", "or", "allergy", "to", "porcine", "materials" ]
[ 0, 0, 0, 0, 0, 0, 0, 4, 4 ]
NCT02101034
,,71:81:cancer,85:120:cancer,145:160:treatment,167:198:cancer
A history of other malignancy ≤ 1 year previous with the exception of basal cell or squamous cell carcinoma of the skin which were treated with local resection only, carcinoma in situ of the cervix, or synchronous H&N primaries
1
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NCT02162420
1:16:chronic_disease
Acute hepatitis
1
[ "Acute", "hepatitis" ]
[ 2, 2 ]
NCT02579044
,,109:134:treatment
It is permissible for female subjects to take oral contraceptives or other hormonal methods while receiving treatment with everolimus
1
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[ 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 1, 1, 1 ]
NCT02527200
1:32:chronic_disease
Type 2 diabetes mellitus (T2DM)
1
[ "Type", "2", "diabetes", "mellitus", "(", "T2DM", ")" ]
[ 2, 2, 2, 2, 2, 0, 0 ]
NCT02304458
47:63:cancer
Part D3: Patients with relapsed or refractory rhabdomyosarcoma
1
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[ 0, 0, 0, 0, 0, 0, 0, 0, 3 ]
NCT02256631
47:50:chronic_disease,,
Mother with any detectable viral replication (HIV RNA above the limit of detection) at last measurement prior to delivery determined within 30 days of delivery
1
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NCT02578901
71:80:treatment
Having been previously randomized in this study at any stage of their treatment
1
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[ 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 1 ]
NCT01959204
26:34:treatment
Has an indwelling access catheter for blood sampling
1
[ "Has", "an", "indwelling", "access", "catheter", "for", "blood", "sampling" ]
[ 0, 0, 0, 0, 1, 0, 0, 0 ]
NCT02464696
18:28:cancer
Have a diagnosed malignancy
1
[ "Have", "a", "diagnosed", "malignancy" ]
[ 0, 0, 0, 3 ]
NCT01893307
1:6:cancer,26:45:cancer,61:88:chronic_disease
Tumor tissue (primary or cervical metastasis) available for human papilloma virus (HPV)
1
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NCT01989585
38:60:treatment,85:106:treatment,,,245:254:treatment
Patients who are receiving any other investigational agents have received any other investigational drugs within 28 days (or five half-lives, whichever is shorter; with a minimum of 14 days from the last dose) preceding the first dose of study treatment and during the study
1
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NCT02496585
7:30:treatment,
Other investigational therapy received within 8 weeks prior to screening visit
1
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[ 0, 1, 1, 0, 0, 0, 0, 0, 0, 0, 0 ]
NCT01763970
,,79:88:treatment
refusal of women of child bearing potential to take a pregnancy test prior to treatment
1
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[ 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 0, 1 ]
NCT02449980
,,,70:82:chronic_disease
Children ages 5 to 18 with clinical diagnosis of primary spontaneous pneumothorax (symptoms of chest pain and/or shortness of breath and pneumothorax demonstrated on chest radiograph) and no prior history of pneumothorax
1
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NCT02762266
,,37:46:treatment
with score =< 9 ((within 4 weeks of treatment)
1
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NCT01925378
28:39:chronic_disease,44:60:chronic_disease,76:93:chronic_disease
Patients with a chronic or acute renal, or hepatic disorder, a significant bleeding disorder, or any other condition which in the Investigator's opinion might preclude study participation for the duration of the trial
1
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NCT01639508
,,,,,342:355:treatment,,,,
The subject is capable of understanding and complying with the protocol requirements and has signed the informed consent document. Sexually active subjects (men and women) must agree to use medically accepted barrier methods of contraception (eg, male or female condom) during the course of the study and for 4 months after the last dose of study drug(s), even if oral contraceptives are also used. All subjects of reproductive potential must agree to use both a barrier method and a second method of birth control. Women of childbearing potential must have a negative pregnancy test at screening
1
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