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NCT03114319 | 24:39:chronic_disease | Clinically significant cardiac disease | 2 | [
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NCT02558010 | 1:19:chronic_disease | Bleeding disorders | 2 | [
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NCT01660607 | 11:33:cancer | High risk acute myeloid leukemia in CR1 | 2 | [
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NCT02073097 | 7:19:cancer,,74:97:cancer,101:106:cancer,110:146:cancer,160:175:cancer,182:198:treatment | Other malignancies within the past 3 years except for adequately treated carcinoma of the cervix or basal or squamous cell carcinomas of the skin, or low-risk prostate cancer after curative therapy | 2 | [
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NCT02646787 | 19:27:chronic_disease,29:38:chronic_disease,54:76:chronic_disease | Not demonstrating delirium, psychosis or any form of Organic Brain Disorder | 2 | [
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NCT02910700 | 38:55:chronic_disease,59:76:chronic_disease,88:114:chronic_disease | Known history of a positive test for hepatitis B virus or hepatitis C virus indicating acute or chronic infection | 2 | [
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NCT02278250 | 84:95:cancer,110:126:treatment,,232:258:treatment,300:311:treatment,327:338:treatment,357:366:treatment | Participants with one histologically or cytologically confirmed malignant advanced solid tumor, for which no standard therapy is available which may convey clinical benefit and/or participants must have progressed after at least 1 prior chemotherapy regimen in the metastatic setting, and for which carboplatin (for Part... | 2 | [
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NCT02427581 | 7:25:cancer | Known metastatic disease | 2 | [
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NCT03037983 | 1:16:chronic_disease | unstable angina | 2 | [
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NCT02469857 | 31:43:treatment,47:77:treatment,87:118:treatment,123:129:cancer,134:155:cancer | Receiving or about to receive chemotherapy or biologic anti-cancer treatment although hormonal manipulation therapies for breast and prostate malignancies are permitted | 2 | [
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NCT01928576 | 24:48:cancer | Patients with advanced malignant hepatic tumors | 2 | [
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NCT02476409 | 32:41:allergy_name | History of hypersensitivity to tolvaptan | 2 | [
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NCT02682147 | 38:48:allergy_name | Prior history of hypersensitivity to Sildenafil | 2 | [
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NCT02538198 | 11:31:treatment | Permitted concurrent therapies | 2 | [
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NCT02100891 | 11:33:cancer,29:32:cancer,105:110:cancer,173:180:treatment,196:225:treatment,227:238:treatment,244:264:treatment,272:279:treatment,283:295:treatment | High-Risk Rhabdomyosarcoma (RMS) or Intermediate Risk Alveolar RMS recurring as more than loco-regional tumor: Must have progressed on or recurred after standard frontline therapy which includes chemotherapy with vincristine, actinomycin, and cyclophosphamide AND either surgery or radiotherapy | 2 | [
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NCT02498301 | 13:27:chronic_disease, | Subject has acute diarrhea within 7 days prior to enrollment | 2 | [
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NCT02343549 | 44:55:allergy_name | Known hypersensitivity to any component of bevacizumab | 2 | [
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NCT02947347 | 1:19:chronic_disease | Measurable disease | 2 | [
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NCT01618357 | 1:30:chronic_disease | Active uncontrolled infection | 2 | [
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NCT02312518 | 1:11:chronic_disease | vasculitis | 2 | [
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NCT01878617 | 13:25:treatment,18:25:treatment,27:39:treatment,49:60:cancer,89:111:treatment,116:123:treatment | No previous radiotherapy, chemotherapy or other brain tumor directed therapy other than corticosteroid therapy and surgery | 2 | [
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NCT02269293 | ,41:54:treatment,62:72:treatment,74:85:treatment,87:98:treatment,100:127:treatment,138:153:treatment | At least 4 weeks must have lapsed since major surgery (e.g., laparotomy, laparoscopy, thoracotomy, video assisted thoracoscopy) prior to study treatment initiation | 2 | [
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NCT03109210 | 11:31:chronic_disease,39:55:chronic_disease,122:132:treatment | untreated psychiatric disorder (e.g., major depression) found on structured interviews as these conditions have specific treatments and it would be inappropriate not to offer those treatments | 2 | [
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NCT00670358 | 15:27:treatment,29:41:treatment,46:59:treatment,79:89:cancer | No concurrent radiotherapy, chemotherapy, or immunotherapy for another active malignancy | 2 | [
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NCT02265315 | 8:26:treatment, | Stable medication therapy for at least 3 months | 2 | [
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NCT02369406 | 1:14:chronic_disease, | HIV-infection documented within 42 days after birth | 2 | [
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NCT01434316 | 1:24:treatment | Prior radiation therapy | 2 | [
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NCT02633163 | 1:14:chronic_disease,,46:55:chronic_disease,85:96:treatment,100:125:treatment, | Herpes zoster within the past 90 days or any infection requiring hospitalization or intravenous or intramuscular antibiotics within the past 60 days | 2 | [
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NCT02079857 | 14:17:chronic_disease | Diagnosis of IBS based on ROME III criteria | 2 | [
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NCT02516813 | 1:9:treatment,,78:84:cancer,178:187:treatment,208:213:cancer,258:277:cancer | Prior RT to the same region within 12 months (Phase Ia, Arm A; subjects with tumors localized in the head and neck region or thorax) or at any time previously (Phase Ia, Arm B; treatment-naïve subjects with SCCHN and Phase Ib; treatment-naïve subjects with Stage III A/B NSCLC or SCCHN) | 2 | [
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NCT03087903 | 15:40:chronic_disease,54:88:treatment,100:131:treatment | Patients with hormone sensitive disease who received prior androgen deprivation therapy as part of primary/salvage local treatment | 2 | [
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NCT02676193 | 67:83:chronic_disease | Marked organic impairment or unstable medical problems (such as a seizure disorder) | 2 | [
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NCT01891318 | 34:56:cancer | Imaging or cytologic evidence of leptomeningeal disease | 2 | [
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NCT03182075 | 1:34:chronic_disease | psychiatric or medical conditions that make participation unsafe | 2 | [
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NCT02315196 | 28:47:treatment,49:61:treatment,66:82:treatment | patients who have received corneal transplants, cadaver skin, or bone transplants are eligible | 2 | [
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NCT02132598 | 1:25:chronic_disease | Cardiovascular disorders | 2 | [
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NCT02562040 | 1:33:chronic_disease,42:57:chronic_disease,63:87:chronic_disease | Severe cardiopulmonary disorders such as cystic fibrosis, and congenital heart disease | 2 | [
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NCT03136029 | ,24:57:treatment | Women currently taking hormone replacement therapy (HRT) | 2 | [
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NCT02513485 | 1:18:chronic_disease,25:41:chronic_disease,45:83:chronic_disease | Chronic infection (e.g. hepatitis B or C or Human Immunodeficiency Virus infection) | 2 | [
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NCT02362308 | 13:35:treatment | status-post surgical sterilization | 2 | [
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NCT02669173 | 1:23:treatment | cytotoxic chemotherapy | 2 | [
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NCT02502006 | 12:18:cancer, | History of cancer within the last 5 years | 2 | [
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NCT03085095 | 36:54:cancer | Newly diagnosed androgen-sensitive metastatic disease | 2 | [
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NCT01600040 | 1:15:cancer | carcinosarcoma | 2 | [
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NCT02356861 | 36:40:chronic_disease | Must meet screening criteria for a PTSD diagnosis | 2 | [
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NCT03120728 | 12:37:chronic_disease | history of peripartum cardiomyopathy | 2 | [
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NCT02106598 | 1:28:chronic_disease | chronic renal insufficiency | 2 | [
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NCT02422641 | 1:11:treatment,15:44:treatment,46:58:treatment,60:72:treatment,76:102:treatment,129:142:cancer | Concurrent or planned systemic chemotherapy, radiotherapy, new hormonal or anti-HER2 directed therapy directed at management of breast cancer | 2 | [
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NCT01676259 | 20:44:cancer | adequately treated non-melanoma skin cancer | 2 | [
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NCT02520791 | 24:66:treatment | Relapsed or refractory post autologous cell transplantation (HCT) | 2 | [
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NCT02177695 | ,,14:27:chronic_disease,, | Class III/IV heart failure or known left ventricular ejection fraction (LVEF) < 50% | 2 | [
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NCT02277613 | 41:67:treatment | Anticipated need for additional planned coronary revascularization procedure(s) | 2 | [
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NCT00147056 | 8:15:treatment,,,91:106:treatment,,127:136:treatment | Use of Avastin in the preceding two weeks or planned use in the forthcoming two weeks and VEGF inhibitors within + 30 days of treatment | 2 | [
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NCT02553161 | 45:63:chronic_disease | has at least one first degree relative with Bipolar I Disorder, as assessed by the Structured Clinical Interview for DSM (SCID; First et al. 1995), the Kiddie Schedule for Affective Disorders and Schizophrenia (KSADS-PL, Kaufman et al., 1997), and the Family History-Research Diagnostic Criteria (FH-RDC; Andreasen et al... | 2 | [
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NCT00914823 | 18:29:treatment,34:61:treatment | seasonal allergy medications and hormone replacement therapy | 2 | [
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NCT02124902 | 14:34:chronic_disease,66:93:chronic_disease,107:131:chronic_disease,133:157:chronic_disease,159:177:chronic_disease,182:201:chronic_disease | Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements | 2 | [
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NCT02046330 | 29:52:treatment, | On a stable drug regimen of psychotropic medication for at least 6 weeks at the time of entry into the study | 2 | [
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NCT02851758 | 7:29:chronic_disease | Known mitochondria disorders | 2 | [
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NCT01631617 | 46:56:treatment,57:82:treatment,84:105:treatment,110:137:treatment | Subjects receiving or planning to receive an IND agent, ultraviolet light therapy, monoclonal antibodies, or systemic immunosuppressants | 2 | [
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NCT02649790 | ,33:36:cancer | IPSS low or intermediate-1 risk MDS | 2 | [
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NCT02276716 | 17:31:treatment,41:49:treatment,51:58:treatment,60:67:treatment,69:83:treatment,85:96:treatment,100:111:treatment | Patients taking anticoagulants, such as warfarin, heparin, aspirin, pentoxifylline, clopidogrel or ticlopidine | 2 | [
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NCT03097588 | 125:135:allergy_name,137:149:allergy_name,151:164:allergy_name | Subjects with known hypersensitivity or other allergic reactions attributed to compounds of similar biologic composition to netupitant, palonosetron, dexamethasone, or other agents used in the study | 2 | [
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NCT03120585 | 56:76:treatment | Those neonates who are intubated for administration of exogenous surfactant but who are immediately extubated to non-invasive respiratory support after surfactant administration will remain eligible for study inclusion | 2 | [
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NCT02451553 | 1:13:treatment,6:13:treatment,,64:73:treatment,102:115:cancer, | Radiotherapy within 4 weeks prior to therapy except palliative radiation to target organs other than primary tumor may be allowed up to 2 weeks prior to registration | 2 | [
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NCT01754857 | 26:60:cancer,61:93:cancer | Histologically confirmed chronic lymphocytic leukemia (CLL)/small lymphocytic lymphoma (SLL) | 2 | [
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NCT01648023 | 54:64:allergy_name,66:77:allergy_name,82:91:allergy_name | Patients with prior contraindications for the use of irinotecan, gemcitabine, or cisplatin | 2 | [
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NCT02079181 | 18:24:cancer | Have one or more tumors visualized by conventional PET-CT, CT or magnetic resonance imaging (MRI) prior to the PET FMAU study | 2 | [
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NCT02249039 | 28:52:chronic_disease | Postoperative from complex congenital heart disease | 2 | [
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NCT01532687 | 17:34:chronic_disease,36:44:chronic_disease,49:54:chronic_disease,75:93:treatment | presence of any non-healing wound, fracture, or ulcer (procedures such as catheter placement not considered to be major | 2 | [
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NCT02192359 | 31:37:treatment,47:55:treatment,57:68:treatment,70:79:treatment,84:96:treatment,,131:146:treatment | Use of drugs known to inhibit UGT1A1, such as atazanir, gemfibrozil, indinavir, or ketoconazole, within 2 weeks prior to start of study treatment | 2 | [
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NCT02064036 | 32:49:allergy_name | Prior allergic reaction to the hormones involved in this protocol | 2 | [
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NCT02408406 | 67:82:treatment | Current outpatient status (participation will be suspended during hospitalization) | 2 | [
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NCT02564978 | 1:18:chronic_disease | Pathologic myopia | 2 | [
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NCT01459107 | 75:108:treatment | Patient agrees to comply with the protocol and states a dedication to the immunomodulatory treatment regime | 2 | [
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NCT02520778 | 32:39:allergy_name | History of hypersensitivity to AZD9291 (or drugs with a similar chemical structure or class to AZD9291) or any excipients of these agents | 2 | [
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NCT02776059 | 1:14:chronic_disease | Renal failure | 2 | [
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NCT02834403 | 19:41:treatment | Concurrent use of potent CYP3A4 inducers | 2 | [
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NCT01505062 | 39:60:treatment,75:98:treatment,,130:137:treatment | Current or anticipated treatment with anticoagulant therapy or the use of anticoagulation therapy within the four weeks prior to surgery | 2 | [
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NCT01917929 | 16:72:treatment | Patient has an existing total hip replacement on the contralateral side | 2 | [
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"an",
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"total",
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"replacement",
"on",
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] | [
0,
0,
0,
1,
1,
1,
1,
1,
1,
1,
1
] |
NCT02165007 | 22:41:chronic_disease | Patients with severe sickle cell disease | 2 | [
"Patients",
"with",
"severe",
"sickle",
"cell",
"disease"
] | [
0,
0,
0,
2,
2,
2
] |
NCT01738009 | 34:37:chronic_disease | Normal subjects or patients with OSA | 2 | [
"Normal",
"subjects",
"or",
"patients",
"with",
"OSA"
] | [
0,
0,
0,
0,
0,
2
] |
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