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NCT02402647 | 1:18:chronic_disease | Hoarding Disorder diagnosis outlined by the Diagnostic and Statistical Manual of Mental Disorders | 2 | [
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NCT01600131 | 75:81:chronic_disease,, | provide the majority of care for a Veteran who has a primary diagnosis of stroke (ICD9 codes for stroke: 430-438) | 2 | [
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NCT02171104 | 1:33:chronic_disease | MPS VI (Maroteaux-Lamy syndrome) | 2 | [
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NCT02907983 | 10:25:treatment | for whom hormone therapy is contraindicated | 2 | [
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NCT03058029 | 1:18:treatment, | Blood transfusion within three (3) months prior to Screening Visit | 2 | [
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NCT02562716 | 10:20:cancer,62:67:cancer,72:85:cancer,87:98:cancer,92:98:cancer,100:123:cancer,125:166:cancer,227:236:treatment, | No prior malignancy is allowed except for adequately treated basal (or squamous cell) skin cancer, in situ cervical cancer, in situ breast (ductal or lobular) cancer, or other cancer for which the patient has been disease and treatment-free for two years | 2 | [
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NCT01990209 | 15:46:cancer | Patients with metastases limited to the bones | 2 | [
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NCT01433315 | 61:75:treatment,77:87:treatment,89:101:treatment,103:116:treatment,118:128:treatment | On no prescription medications other than second generation antihistamines (Cetirizine, Fexofenadine, Desloratadine, Loratadine, etc), oral contraceptive pills, or intrauterine devices | 2 | [
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NCT02206945 | 1:22:chronic_disease | severe claustrophobia | 2 | [
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NCT01515527 | ,,58:75:treatment | Patients aged < 60 years who are unsuitable for standard induction therapy may be eligible after discussion with PI | 2 | [
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NCT02554903 | 1:35:treatment,43:51:treatment,53:65:treatment,70:82:treatment,,126:135:treatment | Treatment with inhaled prostanoids (e.g., iloprost, epoprostenol) or nitric oxide within 24 h prior to Baseline RHC or study treatment initiation | 2 | [
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NCT02710331 | 1:17:chronic_disease | Hearing deficits | 2 | [
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NCT02402660 | 26:41:chronic_disease,211:227:treatment,,254:288:chronic_disease | Has active or historical ocular disorder in the primary study eye that, in the opinion of the investigator, may confound assessment of the retina morphologically or functionally (this could include for example cataract surgery within the past 6 months, choroidal neovascularization (CNV) | 2 | [
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NCT02576431 | 30:39:chronic_disease,41:46:chronic_disease,51:67:chronic_disease,78:100:chronic_disease,111:127:chronic_disease | Active uncontrolled systemic bacterial, viral, or fungal infection, unstable cardiovascular disease, or other systemic disease that would limit compliance with study procedures | 2 | [
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NCT02516670 | 25:59:chronic_disease,55:58:chronic_disease,82:93:chronic_disease,98:119:chronic_disease | Have a known history of human immunodeficiency virus (HIV) (HIV 1/2 antibodies), hepatitis B, or hepatitis C infection | 2 | [
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NCT02824276 | 15:34:treatment | candidate for oral opioid therapy as assessed at the BWH Pain Management Center | 2 | [
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NCT02707471 | ,31:34:chronic_disease | within 12 months of beginning AET | 2 | [
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NCT02648282 | 42:45:chronic_disease,47:58:chronic_disease,63:74:chronic_disease | who have known history of infection with HIV, hepatitis B, or hepatitis C | 2 | [
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NCT02332668 | 1:20:treatment,30:39:treatment,41:48:treatment,53:99:treatment,104:111:chronic_disease,115:138:chronic_disease | replacement therapy (such as thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency) is acceptable | 2 | [
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NCT02374333 | 16:36:treatment | relapsed after prior autologous SCT | 2 | [
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NCT00980538 | 79:82:allergy_name | Previously demonstrated clinically significant allergy or hypersensitivity to ETR or to any of the excipients of ETR | 2 | [
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NCT02727972 | 31:35:chronic_disease | Clinical diagnosis of current PTSD as per DSM-IV | 2 | [
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NCT02557321 | 24:29:chronic_disease,33:56:chronic_disease,58:82:chronic_disease,84:89:chronic_disease,91:107:chronic_disease,109:118:chronic_disease,120:133:chronic_disease,135:144:chronic_disease,149:181:chronic_disease | Clinically significant acute or unstable cardiovascular, cerebrovascular (stroke), renal, gastrointestinal, pulmonary, immunological, endocrine, or central nervous system disorders | 2 | [
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NCT03154580 | 1:17:chronic_disease | Major depression that is not substance-induced) | 2 | [
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NCT02456857 | 7:14:treatment,20:31:treatment,33:54:treatment,59:69:treatment | Prior therapy with bevacizumab, liposomal doxorubicin, or everolimus | 2 | [
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NCT02501096 | 9:35:cancer,81:210:treatment,234:245:treatment,276:297:treatment,307:316:treatment | For the renal cell carcinoma (RCC) cohort, participants must have progressed on treatment with an anti- programmed death receptor-1 /programmed death receptor-ligand 1 monoclonal antibody (anti-PD-1/PD-L1 mAb) administered either as monotherapy, or in combination with other checkpoint inhibitors or other therapies | 2 | [
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NCT02514915 | ,,79:106:treatment | Patients with a documented symptomatic lesion size smaller than 3cm requiring clinical surgical resection | 2 | [
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NCT02135588 | 1:39:chronic_disease | Traumatic hemorrhagic pleural effusion | 2 | [
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NCT03112863 | 21:33:treatment, | Those who have used isotretinoin in the last 6 months | 2 | [
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NCT02498613 | 23:35:treatment,39:41:treatment,,79:91:treatment, | Patients who have had chemotherapy or RT within 3 weeks prior to start of the study agents, or those who have not recovered from adverse events due to agents administered more than 3 weeks earlier | 2 | [
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NCT02193191 | 45:64:chronic_disease,111:135:treatment | Patients must have confirmed and measurable Sickle Cell Disease, defined by SS or Sβ thalassemia confirmed by hemoglobin fractionation | 2 | [
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NCT02203695 | 25:38:treatment,40:60:treatment,65:88:treatment | Concurrent use of other antiandrogens, estrogen-like agents, or 5a-reductase inhibitors | 2 | [
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NCT02342782 | 45:113:allergy_name | History of allergic reactions attributed to compounds of similar chemical or biologic composition to basiliximab | 2 | [
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NCT02335242 | 17:20:treatment,53:75:cancer,,,161:171:treatment | Have a required MRI examination to confirm that the lymphatic malformation is present and is greater than 3 cm in diameter in order for the subjects to receive medication, which happens during the initial screening evaluation portion of the trial | 2 | [
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NCT02762773 | 15:63:chronic_disease | Patients with pre-gestational or gestational diabetes mellitus | 2 | [
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NCT01787409 | 15:30:cancer,83:112:cancer,117:133:cancer,137:158:cancer | patients with B cell lymphoma, unclassifiable, with features intermediate between diffuse large B cell lymphoma and Burkitt lymphoma or post-transplant DLBCL are also eligible | 2 | [
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NCT02091999 | 26:78:cancer,86:107:cancer,109:121:cancer,123:129:cancer,134:141:cancer | Histologically confirmed Transitional Cell Carcinoma of the Urothelium (TCCU) (i.e., cancer of the bladder, renal pelvis, ureter, or urethra | 2 | [
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NCT01897259 | 27:39:chronic_disease | conservative treatment of tennis elbow is recommended as standard of care treatment | 2 | [
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NCT02514070 | 33:37:allergy_name,39:48:allergy_name,52:83:allergy_name | Known sensitivity or allergy to fish, shellfish or omega-3 fatty acids supplements | 2 | [
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NCT01893554 | 14:24:treatment,14:34:treatment,,84:104:treatment | Has received salicylate (aspirin) or salicylate-containing products within 28 days prior to inoculation | 2 | [
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NCT02706353 | 43:71:cancer,76:92:cancer,99:114:cancer | Histologically or cytologically confirmed malignant melanoma from skin, or mucosal melanoma (i.e. ocular melanoma subjects are not eligible) | 2 | [
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NCT02389309 | 1:15:treatment,17:28:treatment,30:42:treatment,44:56:treatment,58:66:treatment | Chlorpromazine, haloperidol, mesoridazine, thioridazine, pimozide | 2 | [
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NCT01966367 | 92:123:treatment | Requirement for CD34+ stem cell selection for a second infusion of stem cells following an allogeneic stem cell transplant from a related or unrelated adult donor | 2 | [
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NCT01697371 | 1:15:cancer | CNS metastases | 2 | [
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NCT01220583 | 9:29:treatment, | History/physical examination within 8 weeks prior to registration | 2 | [
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NCT03040778 | 1:29:chronic_disease | extensive retinal hemorrhage | 2 | [
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NCT01861106 | 31:34:cancer,, | The majority of patients with MDS will have less than 5% blasts | 2 | [
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NCT01795573 | 1:4:chronic_disease,17:22:treatment,26:82:treatment,75:81:treatment | HIV negative by ELISA or reverse transcription polymerase chain reaction (RT-PCR) [if ELISA is positive and RT-PCR is negative, the ELISA is considered false positive] | 2 | [
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NCT02094794 | 1:24:treatment | Prior radiation therapy that would exclude the use of TMLI | 2 | [
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NCT02159703 | 75:89:cancer | Presence of close (2 mm) or positive margins PNI on TORS resection of the primary cancer | 2 | [
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NCT02555280 | 1:14:chronic_disease | pars fracture | 2 | [
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NCT03017937 | 8:32:chronic_disease, | Recent penetrating brain trauma (within 6 months) | 2 | [
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NCT01750567 | 24:39:chronic_disease | Patient with confirmed del11q mutation may be included if untreated | 2 | [
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NCT02947945 | 30:42:treatment,44:56:treatment,61:82:treatment, | Subjects who have received a methotrexate, azathioprine, or mycophenolate mofetil induction regimen may be included if on a stable dose for at least 4 weeks prior to visit 1 | 2 | [
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NCT02468453 | 21:58:chronic_disease,60:76:chronic_disease,78:89:chronic_disease,99:117:chronic_disease,124:144:chronic_disease,146:151:chronic_disease | Subject has a known collagen (connective tissue) disorder, vascular disease, scleroderma or other autoimmune disease (i.e. rheumatoid arthritis, lupus) | 2 | [
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NCT01804634 | 15:37:treatment,43:55:treatment,59:80:treatment | Refractory to induction chemotherapy with COG ANBL0532 or standard chemotherapy | 2 | [
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NCT02640638 | 1:24:chronic_disease | Pregestational diabetes | 2 | [
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NCT02122185 | 38:60:treatment | Patients who are receiving any other investigational agents | 2 | [
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NCT02099240 | 67:98:treatment | Isolation of an organism from bone culture that is susceptible to intravenous and oral antibiotic | 2 | [
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NCT01366612 | 19:30:chronic_disease,35:60:chronic_disease,75:84:treatment | Recovery from all hematologic and non-hematology toxicities from previous therapies | 2 | [
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NCT02567266 | 20:52:chronic_disease | Adolescents with a current substance abuse disorder as determined using the ADIS-5-C/P | 2 | [
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NCT02939183 | 34:78:treatment | Currently receiving treatment in another investigational device or drug study | 2 | [
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NCT02974686 | 4:61:treatment | On standard immunosuppression with tacrolimus and prednisone | 2 | [
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NCT02195232 | 22:28:treatment,32:45:treatment,63:78:chronic_disease | Known intolerance of niacin or ascorbic acid (including known G6PD deficiency) | 2 | [
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NCT03033212 | 7:21:treatment,32:43:treatment,44:54:treatment | Prior spinal surgery excluding laminectomy/discectomy | 2 | [
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NCT02615249 | 41:61:treatment,63:72:treatment,76:82:treatment, | Participation in a clinical trial of an investigational drug, treatment or device during this study or 3 weeks prior to inclusion in this study | 2 | [
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NCT02931110 | 19:21:chronic_disease,,,,,, | For subjects with MM, measurable disease with serum monoclonal immunoglobulin protein (M-protein) ≥1 g/dL, or urine M-protein protein ≥200 mg/24 hours, or involved serum free light chain (SFLC) ≥10 mg/dL | 2 | [
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NCT02876302 | 79:90:treatment | Because no dosing or adverse event data are currently available on the use of ruxolitinib in participants | 2 | [
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NCT01433965 | ,62:74:treatment | Lactating females must agree not to breast feed while taking lenalidomide | 2 | [
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NCT01928576 | 24:49:treatment,69:97:treatment,90:97:treatment,104:137:treatment | subject who received a tyrosine kinase inhibitor after failure of a prior platinum-based therapy, that tyrosine kinase inhibitor therapy would count as an additional line of therapy | 2 | [
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NCT02509260 | 1:31:treatment | enterocutaneous fistula repair | 2 | [
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NCT02516969 | 13:31:cancer | Evidence of distant metastases on any staging or imaging modality | 2 | [
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NCT02453373 | 1:25:chronic_disease,, | Ischemic cortical stroke with NIHSS > _5_ | 2 | [
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NCT02389309 | 1:11:treatment,13:20:treatment,22:31:treatment,33:43:treatment | Amiodarone, sotalol, ibutilide, dofetilide | 2 | [
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NCT02876510 | 1:29:chronic_disease | gastrointestinal obstruction | 2 | [
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