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NCT02504866 | 30:33:chronic_disease | Diagnosis of non-penetrating TBI | {
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NCT02469857 | 1:32:chronic_disease,, | Chronic neurological impairment that leads to a neuro mSOFA component ≥2 | {
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NCT00632853 | 1:13:treatment | chemotherapy | {
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NCT03088033 | 25:38:chronic_disease | Presence of significant valve disease defined by the site cardiologist | {
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NCT03054519 | ,,,59:77:treatment | have an ABI > 0.90 with a 20% or higher drop in ABI after heel-rise exercise will be eligible | {
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NCT02533882 | 1:23:chronic_disease, | Cardiovascular disease event within the past six months | {
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NCT02242526 | 12:38:chronic_disease,92:104:chronic_disease,106:109:chronic_disease,111:126:chronic_disease | Absence of chronic medical conditions that will affect the quality of life survey, such as fibromyalgia, SLE, Crohn's disease, etc | {
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NCT02465060 | 1:29:treatment | low molecular weight heparin is permitted for prophylactic or therapeutic use | {
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NCT02843165 | ,,,82:101:treatment | Patient is a pregnant woman (pregnant women are excluded from this study because radiation treatment has known potential for teratogenic or abortifacient effects) | {
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NCT02640638 | 1:15:chronic_disease,, | Morbid Obesity with BMI >49.99 | {
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NCT02343549 | 11:21:cancer | localized basal cell | {
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NCT02452268 | 1:4:chronic_disease | HIV positive patients | {
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NCT01951885 | 1:18:cancer | Hodgkin's disease | {
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NCT02664909 | 12:22:chronic_disease | History of hemophilia | {
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NCT01898793 | 46:58:allergy_name | Known hypersensitivity to one or more of the study agents | {
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NCT03072381 | 68:74:treatment | self-reported failure of at least 2 of the most common treatments (NSAIDs, relative rest, ice, bracing) for CLE | {
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NCT00678145 | 5:13:chronic_disease | Non-diabetic individuals | {
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NCT02019641 | 1:27:chronic_disease | Severe psychiatric disease | {
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NCT02169830 | 1:14:treatment,16:50:treatment,59:69:treatment | Nortriptyline: monoamine oxidase inhibitors (MAO) such as phenelzine | {
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NCT02598713 | 1:18:chronic_disease | Status asthmatics | {
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NCT00788164 | 1:27:chronic_disease | Human papillomavirus (HPV) 16-positive disease by PCR | {
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NCT02527265 | 35:41:chronic_disease,76:93:chronic_disease,109:120:treatment | History of physician diagnosis of asthma or any other clinically important pulmonary disease, or use of any medications to treat such conditions within the last year | {
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NCT02566928 | 39:43:chronic_disease | presents with signs and symptoms of a SSTI | {
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NCT01983462 | 8:27:treatment,36:49:treatment,51:58:treatment,60:69:treatment,80:89:treatment,92:100:treatment | Taking thyroid medications such as levothyroxine (Levoxyl, Synthroid, Levoxyl, Unithroid); Levodopa | {
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NCT02355002 | 46:51:treatment, | Use of other psychotropic medications (e.g., SSRIs) will be allowed provided the dose has been stable for > 12 weeks | {
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NCT03016130 | 21:51:treatment,, | patients undergoing reduced intensity conditioning, only those regimens in which the expected neutropenia is ≥ 7 days are permitted and the patient must reside in the hospital | {
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NCT02589340 | 1:20:chronic_disease | Parkinson's disease diagnosis | {
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NCT01239160 | 21:111:cancer | have a diagnosis of primary or secondary late Stage 2 or 3 unilateral or bilateral lower extremity lymphoedema | {
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NCT00980538 | 50:62:chronic_disease,64:83:chronic_disease,238:247:treatment,253:256:treatment | Any active clinically significant disease (e.g., pancreatitis, cardiac dysfunction) or findings of medical history, laboratory or physical examination that, in the investigator's opinion, would compromise the participant's safety during treatment with ETR | {
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NCT03121586 | 59:70:chronic_disease,72:82:chronic_disease,84:98:chronic_disease,100:111:chronic_disease,113:129:chronic_disease,131:136:chronic_disease,138:145:chronic_disease,147:158:chronic_disease,169:185:chronic_disease,197:203:cancer,207:219:cancer | Patient has current evidence of a serious and/or unstable psychiatric, neurologic, cardiovascular, respiratory, gastrointestinal, renal, hepatic, hematologic, or other medical disorder, including cancer or malignancies, which would affect the patient's ability to participate in the program | {
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NCT02423863 | ,,,,128:143:treatment | Transaminases ≤ 2 times above the upper limits of the institutional normal, - INR<2 (international normalized ratio) if off of anticoagulation | {
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NCT03065465 | 32:44:chronic_disease | Presence of a benign appearing peptic ulcer | {
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NCT02553265 | 24:26:chronic_disease | Confirmed diagnosis of FD (genetic testing) | {
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NCT01422005 | 26:43:chronic_disease | Subjects must have had a unilateral stroke | {
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NCT02347891 | ,,,,,,78:86:chronic_disease,,,,,,,,,, | Presence of positive autoantibody (ANA >1:80 or RNP or SSA/SSB or any of the myositis specific autoantibody: antisynthetase autoantibodies (anti-Jo-1, PL-7, PL-12, EJ, OJ, KS), anti-SRP, anti-Mi-2, anti-p140) | {
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NCT02911831 | 21:48:chronic_disease,65:80:chronic_disease,92:114:chronic_disease,118:136:chronic_disease | Patients with known bleeding/clotting disorders or a history of thromboembolism (including deep venous thrombosis or pulmonary embolism) | {
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NCT02101736 | ,,,98:107:treatment | Hemoptysis of ≥0.5 teaspoon (2.5 mL) of red blood within 3 months before the first dose of study treatment | {
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NCT03137771 | 20:36:treatment,38:68:treatment,74:79:cancer | Patients receiving targeted therapy (non-cytotoxic systemic therapy) for NSCLC in the first-line setting | {
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NCT00788164 | 1:16:treatment,21:27:treatment,38:80:chronic_disease | Colposcopically and biopsy confirmed grade 3 cervical intraepithelial neoplasia | {
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NCT01568918 | 1:19:treatment | Lumbar Laminectomy | {
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NCT02584309 | 1:31:cancer | Malignant fibrous histiocytoma | {
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NCT02415660 | 16:33:chronic_disease,43:70:treatment,75:78:treatment,110:122:chronic_disease,124:142:chronic_disease,146:170:treatment | History of any systemic disorder in which thoracic spine manipulation and TDN would be contraindicated (i.e. osteoporosis, bleeding disorders or anticoagulant medication use) | {
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NCT03050801 | 13:55:chronic_disease,85:91:chronic_disease,93:110:chronic_disease,112:129:chronic_disease,131:144:chronic_disease,148:164:chronic_disease | Any current major neurological or psychiatric disorder such as (but not limited to) stroke, Parkinson disease, Alzheimer disease, schizophrenia or major depression | {
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NCT02741180 | 18:40:chronic_disease | History of prior cardiovascular disease or significant risk factors | {
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NCT02533674 | 1:18:cancer | Urothelial cancer | {
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NCT03104725 | 10:43:treatment | Taking a monoamine oxidase (MAO) inhibitor | {
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NCT01880567 | 14:26:chronic_disease,41:58:chronic_disease,67:102:chronic_disease,104:120:chronic_disease,131:140:treatment,146:166:treatment,168:177:treatment,181:198:treatment,200:217:chronic_disease,222:241:chronic_disease | uncontrolled hypertension, uncontrolled diabetes mellitus, active/symptomatic coronary artery disease, active infection requiring treatment with systemic antibiotics, antiviral or antifungal agents, active hemorrhage, or psychiatric illness | {
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NCT02140255 | 15:19:treatment, | No receipt of ARVs during the current pregnancy | {
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NCT02451423 | 82:90:allergy_name,94:114:allergy_name,118:133:allergy_name | History of severe allergic, anaphylactic, or other hypersensitivity reactions to chimeric or humanized antibodies or fusion proteins | {
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NCT02421380 | 10:34:chronic_disease | unstable cardiovascular condition | {
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NCT02837510 | 1:20:treatment | Anti-anxiety agents | {
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NCT02312518 | ,,88:97:treatment | Greater than 30% reduction in wound size during the first two weeks of observation and treatment by the investigator | {
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NCT02286687 | ,36:45:treatment,36:152:treatment,112:120:treatment,122:132:treatment,137:152:treatment, | Patients must be >= 4 weeks beyond treatment with any chemotherapy or other investigational therapy to include hormonal, biological, or targeted agents; or at least 5 half-lives from hormonal, biological, or targeted agents, whichever is shorter at the time of treatment initiation | {
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NCT03129542 | 1:24:treatment | Fludrocortisone acetate is a current home medication | {
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NCT02152995 | 20:23:chronic_disease,28:31:chronic_disease,32:41:chronic_disease | chronic or cleared HBV and HCV infection | {
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NCT01312857 | 23:38:treatment,39:55:treatment,102:111:treatment | Patients who have had prior anti EGFR antibody therapy inhibitors and who have not responded to this treatment will be excluded | {
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NCT01742182 | 13:23:chronic_disease,, | Presence of depression defined as the Beck Depression Inventory (BDI) score >14 | {
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NCT02393794 | 1:20:treatment,22:57:treatment,59:68:treatment,72:84:treatment | herapy with heparin, low molecular weight heparin (LMWH), Factor Xa or fondaparinux is allowed | {
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NCT02932410 | ,41:64:treatment | Subjects receiving a combination of > 2 PAH-specific treatments at randomization | {
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NCT02926248 | 20:33:treatment | Patients requiring bilateral MUA | {
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NCT02568267 | 7:32:chronic_disease,47:55:chronic_disease,105:116:chronic_disease | Known interstitial lung disease, interstitial fibrosis, or history of tyrosine kinase inhibitor-induced pneumonitis | {
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NCT02908841 | ,40:52:treatment | Women scheduled for standard multiport laparoscopic | {
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NCT02592707 | 22:36:cancer,102:147:cancer,152:175:cancer | unresectable typical lung carcinoid or atypical lung carcinoid are acceptable (with the exception of Large Cell Bronchial Neuroendocrine Neoplasms and Small Cell Lung Cancers) (Caplin 2015) | {
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NCT02146924 | 30:43:treatment | he/she must have appropriate venous access | {
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NCT03006770 | 8:18:cancer | Active malignancy | {
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NCT02122081 | 31:65:chronic_disease | Patients seropositive for the human immunodeficiency virus (HIV) | {
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NCT02416206 | ,43:55:treatment | Within 9 months of the start of induction chemotherapy and no evidence of relapse or progression | {
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NCT02254863 | 14:23:chronic_disease,25:30:chronic_disease,35:51:chronic_disease,67:89:treatment | Uncontrolled bacterial, viral, or fungal infection at the time of pre-UCBT cytoreduction | {
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NCT02423772 | 65:78:chronic_disease,80:99:chronic_disease,101:110:chronic_disease,114:136:chronic_disease | Meet diagnostic criteria for a current or past DSM diagnosis of schizophrenia, delusional disorder, psychotic or dissociative disorders | {
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NCT00967577 | 18:21:chronic_disease | Known history of HIV | {
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NCT01538966 | 23:35:cancer | The patient harbors a macroadenoma with visual field defects due to chiasmatic compression | {
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NCT02592551 | 28:46:chronic_disease, | Active or prior documented autoimmune disease within the past 2 years | {
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NCT01582191 | 32:42:allergy_name,44:51:allergy_name,53:68:allergy_name,77:105:allergy_name | History of hypersensitivity to vandetanib, lactose, murine products, or any component of the formulation | {
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NCT02187848 | 1:32:treatment | Prior therapy targeting CEACAM5 | {
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NCT02466126 | 13:20:chronic_disease,22:31:chronic_disease,35:60:chronic_disease | presence of bipolar, psychotic or substance-abuse disorders | {
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NCT01174108 | ,,110:114:treatment | ECOG performance status of 3 or more (See Bone & Marrow Transplant Consortium Supportive Care Guidelines for HSCT Recipients) | {
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NCT02496208 | 1:16:treatment,22:33:treatment,26:33:treatment,176:196:cancer | Prior treatment with any therapy on the programmed cell death 1 (PD-1)/PD-L1 axis or anti-cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) inhibitors unless enrolling the urothelial carcinoma with previous checkpoint inhibition therapy expansion cohort | {
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NCT02158793 | 19:37:chronic_disease,51:79:chronic_disease,91:121:chronic_disease | Subjects with any cognitive deficits related to a TBI (traumatic brain injury) and or any organic neurological disorders will not be considered for this protocol | {
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NCT02004275 | ,,,,199:211:treatment | Must have a negative serum or urine pregnancy test with a sensitivity of at least 25 mlU/ml no more than 14 days prior to registration and must agree to repeat this test within 24 hours of starting pomalidomide | {
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NCT03159936 | 1:17:treatment, | Systemic therapy is allowed if on a stable dose and using for at least 3 months -background therapies outlined in Protocol | {
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NCT02520791 | 43:61:chronic_disease | Patients with active, known, or suspected autoimmune disease | {
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NCT01434316 | 7:19:treatment | Prior chemotherapy | {
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NCT02140255 | 24:28:treatment, | Mother did not receive ARVs during the current pregnancy per criteria above | {
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NCT00929006 | 39:49:treatment | Restrictions on use of other drugs or treatments | {
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NCT03096418 | 33:68:treatment | Patients must be candidates for neoadjuvant paclitaxel chemotherapy by their treating oncologist | {
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NCT03113825 | 1:27:treatment,31:41:treatment,44:48:treatment,52:56:treatment,64:74:treatment | Primary surgical treatment is lumpectomy + SLNB or ALND --or-- mastectomy + ALND | {
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NCT01787409 | 30:55:treatment | Capable of swallowing intact study medication capsules | {
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NCT02508038 | 10:14:chronic_disease,26:30:chronic_disease,42:45:chronic_disease | MPX for: HepB (HBV-PCR), HepC (HCV-PCR), HIV (HIV-PCR) | {
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NCT02564744 | 122:130:cancer | Participants must have evaluable or measurable disease in accordance with the International Working Group Guidelines for Lymphoma | {
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NCT01037790 | 74:87:treatment, | The subject has not recovered from clinically-meaningful toxicity due to prior therapy (i.e., back to baseline or Grade ≤ 1) | {
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NCT02058095 | 34:58:chronic_disease | no clinical signs or symptoms of congestive heart failure | {
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NCT02838797 | 16:40:treatment,81:92:treatment,102:113:treatment,115:131:treatment,136:169:treatment,174:193:chronic_disease | history of any gastrointestinal surgery that might impact drug absorption (e.g. gastrectomy), use of apomorphine, anticholinergics, or carbidopa/levodopa intestinal gel for Parkinson's Disease | {
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NCT02367196 | 1:21:cancer,23:31:cancer,35:48:cancer,51:71:cancer | High grade lymphomas (Burkitts or lymphoblastic), plasma cell leukemia | {
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NCT02278315 | 1:16:treatment,40:60:treatment,65:80:treatment | Prior treatment with or intolerance to proteasome inhibitor and immunomodulator | {
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NCT02581215 | 29:38:treatment | Known allergy to any of the treatment components | {
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NCT02287558 | ,,,,,,205:217:treatment,,, | Females of childbearing potential (FCBP)† must have a negative serum or urine pregnancy test with a sensitivity of at least 25 mIU/mL within 10 - 14 days prior to and again within 24 hours of prescribing pomalidomide and must either commit to continued abstinence from heterosexual intercourse or begin TWO acceptable me... | {
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NCT02424968 | ,,157:167:cancer | diagnosed > 5 years ago without evidence of disease, OR treated =< 5 years ago but have a greater than 50% chance of life expectancy of >= 5 years for that malignancy | {
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NCT02746458 | ,173:192:treatment | Additional fracture, dislocations or soft tissue injuries to the study limb that would compromise the ability to weight bear as tolerated and initiate PT within 28 days of definitive fixation | {
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NCT02912572 | 8:26:chronic_disease | Active autoimmune disease that might deteriorate when receiving an immunostimulatory agent | {
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NCT03179449 | 27:38:allergy_name | Known hypersensitivity to ferumoxytol or any of its components | {
"allergy_name": "ferumoxytol",
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