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NCT02124902 | 1:11:cancer,15:50:cancer,99:130:cancer | basal cell or squamous cell carcinoma of the skin which were treated with local resection only or carcinoma in situ of the cervix | 3 | [
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NCT02340156 | 9:29:chronic_disease | Serious nonmalignant disease | 3 | [
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NCT01777035 | 8:29:chronic_disease | Severe chronic pain syndrome on admission | 3 | [
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NCT02660528 | 20:39:chronic_disease,46:60:chronic_disease,62:75:chronic_disease,77:92:chronic_disease | Recent exposure to uncommon infections (e.g. histoplasmosis, blastomycosis, coccidiomycosis) through recent travel to the Ohio and Mississippi River Valleys and the Southwest | 3 | [
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NCT02441101 | 35:56:treatment | Left ventricular assist device or heart transplantation | 3 | [
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NCT00719888 | ,,122:153:treatment | Diffusion capacity for carbon monoxide corrected (DLCOcorr) > 50% normal or a pediatric patient who is unable to perform pulmonary function tests (PFTs) but has adequate pulmonary function | 3 | [
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NCT02872857 | 15:32:chronic_disease | Presence of a cerebral aneurysm on computed tomographic angiography (CTA) or Angiogram for which clipping or coiling is possible | 3 | [
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NCT02233868 | 1:17:treatment | anticholinergics | 3 | [
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NCT02270450 | 1:18:chronic_disease | Bowel obstruction below (distal to) ligament of Treitz | 3 | [
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NCT02317991 | 1:12:treatment | open biopsy | 3 | [
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NCT01880567 | 17:20:cancer | Newly Diagnosed MCL: Any serious medical condition that places the patient at unacceptable risk and/or would prevent the subject from signing the informed consent form | 3 | [
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NCT02266329 | 19:42:chronic_disease,50:65:chronic_disease,67:88:chronic_disease,,106:130:chronic_disease,132:177:chronic_disease,179:203:chronic_disease,,,225:248:chronic_disease,,, | Acute or unstable chronic medical illness (e.g., unstable angina, myocardial infarction within 6 months, congestive heart failure, symptomatic or concerning cardiac arrhythmias; pre-existing hypotension (systolic BP<110) or orthostatic hypotension (systolic drop >20 mm mercury (Hg) after 2 min standing accompanied by l... | 3 | [
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NCT00539162 | 1:7:cancer,39:51:treatment,55:72:treatment, | Cancer-free and have not received any chemotherapy or radiation therapy for >/=12 months prior to enrolling on this study | 3 | [
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NCT02134392 | 12:38:chronic_disease | History of inflammatory bowel disease | 3 | [
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NCT02402088 | 1:6:chronic_disease,,, | Obese BMI group: BMI 30-35 as calculated based on height and weight | 3 | [
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NCT02912572 | 20:60:treatment,52:60:treatment,131:151:treatment,,193:203:treatment | Subjects requiring hormone replacement with corticosteroids are eligible if the steroids are administered only for the purpose of hormonal replacement and at doses ≤ 10 mg or 10 mg equivalent prednisone per day | 3 | [
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NCT00967577 | 78:90:cancer,99:114:cancer,159:175:treatment,192:217:treatment | Histologically, or cytologically documented, advanced stage, malignant adult solid tumors (except prostate cancer) that are refractory to, or recurrent from, standard therapy or for which no curative standard therapy exists | 3 | [
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NCT01675154 | 1:37:treatment,9:16:treatment,22:37:treatment,39:46:treatment | Current therapy with anti-coagulants, digoxin and anti-arrhythmics | 3 | [
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NCT02744352 | 1:23:chronic_disease | Chronic pain syndromes | 3 | [
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NCT00358657 | 1:15:chronic_disease | Fanconi anemia | 3 | [
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NCT02213497 | ,,,103:122:treatment,163:165:treatment,169:189:treatment | Patients with primary tumors exceeding 8 cm in length or 5 cm in width ( length should be measured by endoscopic findings, width should be measured by diagnostic CT or CT portion of PET/CT) | 3 | [
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NCT02759211 | 33:35:chronic_disease | Confirmed clinical diagnosis of MS | 3 | [
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NCT02050347 | 13:22:chronic_disease | Mixed donor chimerism (any level) | 3 | [
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NCT02762266 | 15:28:chronic_disease, | Patients with liver disease classified as Child Pugh class A or B | 3 | [
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NCT02127398 | 1:17:chronic_disease,44:65:chronic_disease,85:106:treatment,108:139:treatment | Active infection at other sites (excluding Clostridium difficile) requiring ongoing antibacterial therapy (antiviral or antifungal therapy is acceptable) | 3 | [
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NCT02849639 | 25:36:allergy_name,67:77:allergy_name,81:100:allergy_name,,196:202:treatment | No contraindications to Aβ-PET scan including hypersensitivity to PET ligand or radiation exposures in the past year that would exceed the acceptable safe annual exposure in combination with the Aβ PET | 3 | [
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NCT02520427 | ,,127:137:treatment | Women who are lactating/breastfeeding or who plan to breastfeed while on sudy through 1 week after receiving the last dose of study drug | 3 | [
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NCT02653287 | 110:113:chronic_disease | include meeting at least 4 of 11 American College of Rheumatology (ACR) classification criteria for definite SLE, or 3 out of 11 ACR classification criteria with also meeting at least one SLICC criteria | 3 | [
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NCT01905046 | 23:44:treatment, | Administration of any investigational agent =< 30 days prior to pre-registration | 3 | [
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NCT02390752 | 18:58:cancer | Individuals with malignant peripheral nerve sheath tumors will not be eligible to participate in the phase II portion of the trial | 3 | [
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NCT02169089 | 84:100:treatment,102:115:chronic_disease,117:133:treatment | Any surgical or medical condition which might alter pharmacokinetics of drug (e.g. renal transplant, liver failure, liver transplant) | 3 | [
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NCT02167958 | 1:30:cancer,34:53:cancer,,99:108:treatment,120:140:treatment,168:189:treatment,219:250:treatment | Marginal zone B-cell lymphoma or follicular lymphoma that has progressed after at least two prior therapies (excluding single agent Rituxan) and are ineligible for an autologous transplant or relapsed/progressed after autologous stem cell transplant | 3 | [
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NCT02589600 | ,20:34:treatment,36:45:treatment,50:70:treatment,,,168:183:treatment | Women currently on bisphosphonate, denosumab, or teriparatide therapy or who have been on a bisphosphonate for greater than 1 year during the previous 2 years because bisphosphonates are long acting | 3 | [
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NCT02177695 | 1:26:cancer,28:47:cancer,53:81:cancer | pure small cell carcinoma, pure adenocarcinoma, and pure squamous cell carcinoma histologies | 3 | [
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NCT02192398 | 13:21:treatment,,, | On a stable morphine equivalent dose of at least 60mg/day and ≤ 240mg/day for at least 3 months | 3 | [
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NCT02548351 | 26:35:chronic_disease | Histological presence of cirrhosis | 3 | [
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NCT02414139 | 1:26:treatment | Strong inducers of CYP3A4 | 3 | [
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NCT01883076 | ,70:92:treatment | Child not completing all pre-procedure work-up within 10 days of the Stage II Glenn surgery as listed in section 6 of this protocol AND lack of pre-procedure work-up documented as a safety concern by a site investigator | 3 | [
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NCT02016781 | 1:32:cancer,36:51:cancer,52:79:cancer,94:97:cancer | Chronic myelomonocytic leukemia or myelodysplastic/myeloproliferative neoplasm (unacceptable MDS subtypes) | 3 | [
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NCT02939755 | 16:32:chronic_disease,34:43:chronic_disease,55:72:chronic_disease | no evidence of thought disorder, delusions, or active suicidal ideation is observed or reported | 3 | [
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NCT03078504 | 12:28:treatment | listed for organ transplant | 3 | [
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NCT01430390 | 48:60:cancer,,109:132:treatment,134:143:treatment,145:157:treatment,165:179:treatment | Relapse on this protocol is detection of CD19+ malignancies in bone marrow ≥ 5% or extramedullary lesion by morphology cytogenetics, molecular, radiographic and/or flow cytometry | 3 | [
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NCT01802346 | 1:39:treatment | Prior therapy with inhibitors of IGF-1 | 3 | [
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NCT02632721 | 46:56:treatment | Patients must be eligible for treatment with decitabine | 3 | [
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NCT03048448 | 1:28:chronic_disease,,, | Moderate hepatic impairment (Group 1): Child-Pugh Class B (7-9 points) | 3 | [
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NCT02057133 | 13:22:treatment,,25:36:treatment,84:104:treatment,109:127:cancer,157:181:treatment | For Part F (LY2835219 + trastuzumab):The participant must have received at least 1 chemotherapy regimen for metastatic disease and may be receiving ongoing therapy with trastuzumab | 3 | [
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NCT02573493 | 45:119:allergy_name | History of allergic reactions attributed to compounds of similar chemical or biologic composition to any of the agents used in this study | 3 | [
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NCT02349867 | 50:67:treatment,94:117:chronic_disease,119:154:chronic_disease,156:181:chronic_disease,183:218:chronic_disease,220:239:chronic_disease,268:286:chronic_disease,298:314:chronic_disease | Experienced any of the following toxicities with prior gemcitabine adminstration (if given): capillary leak syndrome, posterior reversible encephalopathy, hemolytic uremic syndrome, thrombotic thrombocytopenic purpura, unexplained dyspnea or other evidence of severe pulmonary toxicity, or severe hepatic toxicity | 3 | [
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NCT00788164 | 1:14:chronic_disease | Lichen planus | 3 | [
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NCT02573493 | 66:69:chronic_disease,128:135:chronic_disease,139:142:treatment | Arm 3: Presence of disease at the oropharynx sub-sites, which is HPV-related as verified by p16, a surrogate marker of HPV, or HPV ISH or PCR | 3 | [
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NCT02657993 | 113:123:treatment | Experiencing ongoing pain and/or stiffness in one or more joints, which started or worsened after initiation of AI therapy | 3 | [
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NCT03040778 | 15:41:chronic_disease | Patients with serious cardiac arrhythmia | 3 | [
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NCT02995733 | 7:11:chronic_disease,48:60:chronic_disease,127:142:chronic_disease,144:169:chronic_disease,188:209:treatment,211:225:chronic_disease,227:234:chronic_disease,240:266:chronic_disease | Dx of COPD in a never smoker without any other lung disease or any other disease that might cause airway obstruction such as: Cystic Fibrosis, Connective Tissue Disease, premature birth, organ transplantation, bronchiectasis, sarcoid, and obliterative bronchiolitis | 3 | [
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NCT02496208 | 1:36:cancer,38:45:cancer,47:53:cancer,55:67:cancer | Urothelial carcinoma of the bladder, urethra, ureter, renal pelvis | 3 | [
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NCT02474199 | 27:30:chronic_disease,34:37:chronic_disease,51:64:treatment | No detectible circulating EBV or CMV DNA prior to Treg infusion, assessed at the time of PBMC collection for manufacture | 3 | [
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NCT03143985 | ,,109:118:treatment,209:212:treatment,216:224:treatment | Men must agree to use a latex or synthetic condom during sexual contact with a FCBP even if they have had a vasectomy from the time of signing the informed consent form through 60 days after the last dose of POM or TEW-7197 | 3 | [
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NCT02287558 | 1:20:chronic_disease,, | Renal insufficiency, serum creatinine > 2.0 mg/dl | 3 | [
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NCT02498951 | 11:23:treatment,,, | high-dose methotrexate is defined as >= 3 grams/m^2; methotrexate dose reduction for creatinine clearance < 100 ml/min is permitted | 3 | [
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NCT02133196 | 12:54:allergy_name | History of severe immediate hypersensitivity reaction to any of the agents used in this study | 3 | [
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NCT02540616 | 5:25:chronic_disease | Any active skin disorder that affects skin integrity of the scalp | 3 | [
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NCT02188745 | 5:35:treatment, | Any investigational cancer therapy in the last 28 days | 3 | [
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NCT02915744 | 14:32:treatment, | Last dose of anticancer therapy must have been administered within 6 months of the date of randomization into this study | 3 | [
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NCT00716066 | 1:35:chronic_disease | Autoimmune cerebellar degeneration | 3 | [
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NCT02233322 | 18:27:treatment,33:42:treatment,47:57:treatment,149:173:chronic_disease | May be receiving treatment with phosphate and calcitriol, but must be willing to undergo dose adjustments by the investigators if iron resolves the phosphate wasting defect | 3 | [
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NCT02385110 | 42:58:chronic_disease,71:81:cancer,100:120:chronic_disease | Any serious/and or unstable pre-existing medical disorder (aside from malignancy exception above), psychiatric disorder, or other conditions that could interfere with subject's safety, obtaining informed consent or compliance to the study procedures | 3 | [
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NCT01953263 | 44:66:chronic_disease,70:90:chronic_disease,102:138:treatment | Patients with evidence or diagnosis of any primary muscle disease or coagulation disorder (including concomitant anti-coagulation therapy) | 3 | [
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NCT01937949 | 1:11:chronic_disease,13:23:chronic_disease,27:67:chronic_disease, | Juxtarenal, suprarenal or type IV thoracoabdominal aortic aneurysm with a diameter ≥ 5.0 cm or 2 times the normal aortic diameter | 3 | [
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NCT00875342 | 8:17:treatment | Use of pacemaker | 3 | [
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NCT01554371 | ,,,152:168:treatment, | Female patient of childbearing potential must have a negative serum or urine pregnancy test β-hCG within 72 hours prior to receiving the first dose of study medication and agree to the use of effective methods of contraception while on study | 3 | [
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NCT02094625 | 1:10:treatment, | Cisplatin must be delivered over <3 day | 3 | [
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NCT02435992 | ,49:66:chronic_disease,68:83:chronic_disease,88:105:chronic_disease | Current or recent (within 3 months) evidence of fulminant colitis, toxic megacolon, or bowel perforation | 3 | [
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NCT01896999 | 29:59:cancer | other histologies including lymphocyte predominant (LP) HL are not permitted | 3 | [
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NCT02151175 | 15:23:chronic_disease,25:33:chronic_disease,38:47:chronic_disease | Subjects with dementia, delirium and psychotic symptoms | 3 | [
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NCT02355535 | 1:26:treatment,31:49:cancer,98:116:treatment,118:145:treatment,147:159:treatment,161:177:treatment,182:205:treatment | Prior systemic treatments for metastatic disease are permitted but may not be ongoing, including targeted therapies, biologic response modifiers, chemotherapy, hormonal therapy, or investigational therapy | 3 | [
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