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NCT01903330 | 26:40:treatment | Anticipation of need for major surgical procedure during the course of the study | 2 | [
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NCT00909909 | 4:31:cancer | No Paget disease of the nipple | 2 | [
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NCT02624765 | 1:20:chronic_disease | sick sinus syndrome | 2 | [
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NCT02374333 | 1:13:chronic_disease,37:44:treatment,110:122:chronic_disease | CNS3 disease that is progressive on therapy, or with CNS parenchymal lesions that might increase the risk of CNS toxicity | 2 | [
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NCT02832115 | 41:50:allergy_name | Hypersensitivity or contraindication to lidocaine | 2 | [
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NCT02516332 | 28:35:chronic_disease,,,,188:203:chronic_disease,205:219:chronic_disease,224:238:chronic_disease | Patients also will have an anxiety symptom severity score of at least 8 on the Hospital Anxiety and Depression-Anxiety scale (HADS-A) or a DSM-5 diagnosis of an Anxiety Disorder, such as General Anxiety, Social Anxiety, or Panic Disorder | 2 | [
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NCT02434809 | 32:38:allergy_name | History of hypersensitivity to nickel | 2 | [
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NCT02451982 | 54:74:chronic_disease | Conditions, including alcohol or drug dependence, or intercurrent illness that would affect the patient's ability to comply with study visits and procedures | 2 | [
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NCT01465100 | 7:34:chronic_disease | Known biopterin synthesis defects | 2 | [
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NCT02081404 | 18:36:treatment | Prior history of esophageal surgery | 2 | [
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NCT02347995 | 11:27:chronic_disease | untreated major depression by clinical interview | 2 | [
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NCT02533674 | 43:54:treatment | Patients who have previously discontinued gemcitabine-containing regimens due to gemcitabine-related toxicity | 2 | [
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NCT02378428 | 106:123:treatment | The presence of mixed response (MR), or no response (NR) following the completion of A3973 or equivalent induction therapy | 2 | [
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NCT02204956 | 1:43:treatment | Mini-Mental State Examination (MMSE: [45]) | 2 | [
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NCT00719888 | 1:29:cancer,31:57:cancer,59:62:cancer,63:66:cancer,69:98:cancer,100:126:cancer,130:149:cancer,,200:215:treatment | Chronic lymphocytic leukemia /small lymphocytic lymphoma (CLL/SLL), marginal zone B-cell lymphoma, lymphoplasmacytic lymphoma or follicular lymphoma that have progressed after at least two different prior therapies | 2 | [
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NCT02075671 | 13:22:chronic_disease | Scarring or infection in the area being treated | 2 | [
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NCT02075671 | 8:31:treatment, | Use of topical corticosteroids (on the face) 1 month prior to Visit 1 | 2 | [
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NCT02319369 | 23:92:treatment | receiving concomitant treatment with a strong inhibitor or inducer of cytochrome P450 3A4/5 | 2 | [
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NCT02549937 | 15:26:treatment | Currently use medications known to cause QT prolongation or Torsades de Pointes | 2 | [
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NCT02167009 | 12:30:treatment | History of pelvic irradiation | 2 | [
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NCT02397083 | 64:115:treatment, | Patients who are currently part of or have participated in any clinical investigation with an investigational drug within 1 month prior to dosing | 2 | [
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NCT02881320 | 11:16:chronic_disease,,,,,, | Cohort 1: HIV-1 infected adolescents (12 to < 18 years of age and screening weight ≥ 35 kg) who are virologically suppressed for ≥ 6 months prior to screening | 2 | [
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NCT02145351 | 9:33:chronic_disease | Complex congenital heart disease | 2 | [
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NCT02496208 | 23:34:chronic_disease | appearance of one new bone lesion | 2 | [
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NCT02607514 | 8:23:chronic_disease | Active suicidal intent within the past year (yes on item 4 or 5 on the Columbia-Suicide Severity Rating Scale) | 2 | [
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NCT00924027 | 1:19:cancer | distant metastases | 2 | [
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NCT02252081 | 12:21:treatment,33:51:treatment,72:81:treatment,85:103:chronic_disease, | History of metformin use or any insulin sensitizer or any drug for the treatment of metabolic syndrome over the last one year | 2 | [
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NCT02952365 | 40:53:treatment | Subjects who have previously undergone LASIK surgery | 2 | [
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NCT02507232 | 31:46:treatment,48:60:treatment,62:74:treatment,85:110:treatment,127:138:cancer | Disease that has not received prior radiation, radiosurgery, chemotherapy, or other investigational treatment directed at the brain tumor at any time. Previous surgical procedures | 2 | [
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NCT01883258 | ,29:56:treatment | postmenopausal women taking hormone replacement therapy | 2 | [
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NCT02342782 | 1:22:treatment,10:22:treatment,26:35:treatment,,87:91:treatment,100:124:treatment,148:177:treatment | Systemic chemotherapy or radiation cannot have been given within 4 weeks prior to the Y-90 dose of radioimmunotherapy (RIT), with the exception of single agent cyclophosphamide priming chemotherapy administered for mobilization | 2 | [
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NCT03051282 | 27:37:chronic_disease | Subject with a history of angioedema | 2 | [
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NCT02525861 | 48:55:chronic_disease,57:68:chronic_disease,73:90:chronic_disease,141:156:chronic_disease,158:183:chronic_disease | The participant has any clinically significant medical, psychiatric, or cognitive illness, or any other uncontrolled medical condition (eg, unstable angina, transient ischemic attack) that, in the opinion of the investigator, would impede the participant's ability to comply with the study procedures, pose increased ris... | 2 | [
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NCT02965638 | 1:13:chronic_disease,17:31:chronic_disease | Fetal mitral or aortic atresia | 2 | [
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NCT02273375 | 47:71:cancer | Histologically confirmed diagnosis of primary non-small cell carcinoma of the lung | 2 | [
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NCT03182907 | 17:44:treatment, | Has received an investigational study agent within the previous 30 days | 2 | [
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NCT02215096 | 24:38:chronic_disease | History or evidence of cardiovascular risk | 2 | [
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NCT02579265 | 1:33:chronic_disease | Cyanotic congenital heart defect | 2 | [
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NCT01835626 | 108:118:treatment | Agreement not to donate blood or blood products during the study and for 7 months after discontinuation of vismodegib | 2 | [
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NCT02480114 | 24:34:treatment | Prior non-tolerance of gabapentin | 2 | [
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NCT02076906 | 15:22:chronic_disease | Defined as no dyspnea at rest | 2 | [
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NCT02429349 | 34:41:cancer,60:78:cancer,87:95:cancer,100:120:cancer | include, but are not limited to, cancers with high risk of ovarian metastasis such as leukemia and non-Hodgkin lymphoma | 2 | [
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NCT02911792 | 1:124:treatment | Ingestion of medications known to interfere with the renin-angiotensin system or renal function, including diuretic therapy | 2 | [
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NCT02466685 | 25:47:treatment,55:62:treatment,64:73:treatment,78:86:treatment, | Individuals receiving a single mood stabilizer (e.g., lithium. valproate, or lamictal) are allowed if a stable dose has been maintained for at least 2 months prior to screening | 2 | [
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NCT02880215 | 17:35:chronic_disease,37:53:chronic_disease,58:71:chronic_disease | current or past psychotic disorder, bipolar disorder, or schizophrenia | 2 | [
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NCT01614197 | 108:119:treatment | Patients with known optic nerve and/or retinal involvement (because it may not be possible to safely delay irradiation) are not eligible | 2 | [
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NCT02320292 | 14:24:cancer,35:44:treatment,106:114:cancer | Active other malignancy requiring treatment that would interfere with the assessments of response of the lymphoma to protocol treatment and would interfere with follow-up assessments through year 5 | 2 | [
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NCT02159495 | 99:123:treatment,131:154:treatment,,,306:321:treatment | Research participant with central nervous system (CNS) leukemic involvement that is refractory to intrathecal chemotherapy and/or cranio-spinal radiation but effectively treated to completion remission (< 5 white blood cell[WBC]/mm^3 and no blast in cerebrospinal fluid [CSF]) is eligible to proceed with lymphodepletion | 2 | [
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NCT01703117 | 6:30:chronic_disease | with mild Alzheimer's disease determined after neurological and neuropsychological evaluation following the National Institute on Aging - Alzheimer's disease Association criteria that recently revisited the NINCDS-ADRDA criteria | 2 | [
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NCT02335242 | 47:69:chronic_disease, | Be required to have the clinical diagnosis of lymphatic malformation that appears to be over 3 cm in greatest diameter in order to be evaluated for entry | 2 | [
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NCT02004275 | 1:13:treatment,14:32:cancer,,122:150:treatment | Lenalidomide-refractory disease is defined as disease progression on or progression within 60 days of the last dose of a lenalidomide-based treatment | 2 | [
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NCT02703220 | 27:45:chronic_disease,117:145:chronic_disease,146:166:chronic_disease,, | Patients with significant pulmonary diseases by history and abnormal pulmonary function testing, including moderate obstructive/restrictive lung/chest wall disorders with resting oxygen saturation of <96% or on supplemental oxygen | 2 | [
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NCT02059239 | 106:117:treatment | History of allergic reactions attributed to compounds of similar chemical or biologic composition to any medications listed in the protocol | 2 | [
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NCT01061515 | ,72:90:treatment | Provided the patient has been allowed at least 4 weeks to recover from surgical debulking, no additional recovery time is required for port placement | 2 | [
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NCT02570984 | 1:11:treatment,15:41:treatment,53:68:treatment | Prior IVIG or systemic immunosuppressant other than corticosteroids | 2 | [
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NCT02080221 | 30:40:cancer,73:82:treatment,,134:147:cancer,164:179:cancer | patients with an early stage malignancy that is not expected to require treatment in the next 2 years (such as early stage, resected breast cancer or asymptomatic prostate cancer) | 2 | [
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NCT02056873 | 42:45:treatment | (Subjects not required to participate in HRT but it will be highly encouraged, and must be completed prior to start of this study's protocol | 2 | [
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NCT02533674 | 22:30:treatment | Prior treatment with PM060184 | 2 | [
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NCT02585973 | ,69:78:treatment,80:97:treatment,101:122:treatment | Receiving or less than 21 days since receiving any other concurrent cytotoxic, biologic agent(s) or investigational agent | 2 | [
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NCT01465100 | 1:13:treatment | Liver biopsy shows significant fibrosis, defined by the Ishak Stage 5 | 2 | [
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NCT01453088 | 1:18:chronic_disease | Organ dysfunction | 2 | [
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NCT02007239 | 38:52:treatment, | Previous administration of any other biologic agent targeted at cytokine blockade within 5 days of enrollment | 2 | [
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NCT02242526 | 1:9:chronic_disease,, | Upper GI with a documented hiatal hernia greater than 5cm | 2 | [
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NCT01871727 | 13:42:chronic_disease | Significant pulmonary symptoms or disease | 2 | [
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NCT01351103 | 1:40:chronic_disease,44:68:chronic_disease,116:127:treatment,169:175:chronic_disease,177:185:chronic_disease,187:195:chronic_disease,197:219:chronic_disease,221:242:treatment | Impairment of gastrointestinal function or gastrointestinal disease that may significantly alter the absorption of oral LGK974 (e.g., ulcerative diseases, uncontrolled nausea, vomiting, diarrhea, malabsorption syndrome, small bowel resection) | 2 | [
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NCT00293475 | 56:66:treatment | cytology (analysis from cerebral spinal fluid [CSF] or vitrectomy) | 2 | [
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NCT02408120 | 1:24:treatment | non-insulin injectables | 2 | [
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NCT01686659 | 45:60:treatment | Adult patients undergoing one of the listed major surgeries associated with possibility of significant blood loss | 2 | [
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NCT02551679 | 58:74:chronic_disease,121:137:treatment,195:215:treatment | Subjects who, in the opinion of the investigator, have a vascular disease prognosis that indicates they would require a major amputation in a time frame shortly after administration of the IMP (investigational drug or placebo) | 2 | [
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NCT02990481 | 1:16:chronic_disease | cardiac disease | 2 | [
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