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NCT01989507 | 49:69:treatment | actively quitting smoking or current use of any nicotine replacement or other smoking cessation treatment | 2 | [
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NCT02727972 | 14:31:chronic_disease,56:70:treatment,80:88:treatment,90:97:treatment,99:106:treatment,108:115:treatment | history of a bleeding disorder or are currently taking anticoagulants (such as Coumadin, Heparin, Pradaxa, Xarelto) | 2 | [
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NCT02588612 | 1:26:treatment,,51:64:treatment,66:98:treatment,,223:243:treatment,,294:340:treatment | Investigational treatment within 4 weeks prior to leukapheresis; experimental anti-cancer vaccine within 2 months prior to leukapheresis in the absence of response or in the opinion of the Investigator is responding to an experimental vaccine given within 6 months prior to leukapheresis; any prior gene therapy using an... | 2 | [
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NCT01045148 | 13:36:cancer | Evidence of distant metastases (M1) | 2 | [
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NCT01961557 | 16:41:chronic_disease | Diagnosed with knee extension deficiency as indicated by a crouched posture during gait lacking | 2 | [
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NCT03071393 | 1:19:chronic_disease | Spinal cord injury affecting segments between C4-T12 | 2 | [
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NCT02737202 | 10:21:chronic_disease,23:28:chronic_disease,30:37:chronic_disease,39:59:chronic_disease,63:81:chronic_disease,, | Advanced hematologic, renal, hepatic, non-LAM lung disease or metabolic diseases; or BMI of >35 | 2 | [
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NCT02844738 | 29:43:chronic_disease | Patients with indication of Osteoarthritis | 2 | [
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NCT02509546 | 1:12:cancer,35:37:treatment,55:62:treatment | De novo AML who have not achieved CR after 2 lines of therapy | 2 | [
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NCT01326715 | 40:46:chronic_disease | Clinically significant iron-deficiency anemia | 2 | [
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NCT02515110 | 27:47:treatment,51:62:treatment | History of ipsilateral or contralateral breast or thoracic RT for any condition | 2 | [
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NCT02977468 | 23:36:chronic_disease | Pathologically proven nodal disease at diagnosis is not allowed | 2 | [
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NCT02383979 | 29:45:treatment | inability to cooperate with physical therapy | 2 | [
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NCT01384513 | 1:31:cancer,54:76:chronic_disease,80:129:chronic_disease | MDS (myelodysplastic syndrome), specific subtypes of RA (refractory anemia) or RARS (refractory anemia with ringed sideroblasts) subtypes | 2 | [
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NCT03053453 | 10:33:treatment | Revision Total Knee Arthroplasty | 2 | [
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NCT02349958 | 21:36:chronic_disease | Patients with known extra-abdominal disease, or unresected bulky abdominal retroperitoneal lymph nodes | 2 | [
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NCT02881242 | 5:18:treatment,20:42:treatment,44:78:treatment,44:56:treatment,80:96:treatment,101:114:treatment,, | Any major surgery, extensive radiotherapy, chemotherapy with delayed toxicity, biologic therapy, or immunotherapy within 30 days of enrollment and/or daily or weekly chemotherapy without the potential for delayed toxicity within 14 days of enrollment | 2 | [
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NCT02774421 | 1:14:cancer | subependymoma | 2 | [
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NCT02807272 | 14:18:cancer | Diagnosis of CMML as defined by the World Health Organization (WHO) criteria | 2 | [
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NCT02171104 | 1:22:chronic_disease | Peroxisomal Disorders | 2 | [
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NCT02310399 | 1:26:chronic_disease | Cochlear nerve deficiency | 2 | [
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NCT02997709 | 15:33:cancer | Patients with metastatic disease are encouraged to participate | 2 | [
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NCT02532621 | 66:79:chronic_disease | Subject currently has a known or suspected bacterial, fungal, or HIV infection | 2 | [
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NCT02210650 | 1:28:chronic_disease | primary hyperparathyroidism | 2 | [
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NCT03100370 | 26:49:treatment | No planned alteration in upper-extremity therapy or medication for muscle tone during the course of the study | 2 | [
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NCT02903511 | 1:18:chronic_disease | Diabetes mellitus | 2 | [
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NCT00977977 | ,,69:99:treatment,101:114:treatment,118:121:treatment, | Nephrotic range proteinuria (>3.5 g/24 hours) that persists despite angiotensin antagonist therapy (ACE inhibitor or ARB) for at least 2 months unless intolerant | 2 | [
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NCT02250664 | 11:31:treatment,33:42:treatment,52:69:treatment | Have used nicotine replacement, bupropion or other pharmacotherapies as cessation aids in the past month | 2 | [
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NCT03059030 | 22:33:treatment | Contraindications to angiography and selective visceral catheterization such as bleeding, diathesis or coagulopathy that is not correctable by usual therapy or hemostatic agents (e.g. closure device) | 2 | [
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NCT02217345 | 1:26:cancer | non-melanoma skin cancers | 2 | [
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NCT02768727 | 23:49:chronic_disease | Current or history of neuropsychiatric disorders | 2 | [
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NCT02349867 | 26:47:chronic_disease,51:75:chronic_disease,87:113:chronic_disease,126:140:treatment,158:167:treatment | embolic events such as a myocardial infarction or cerebrovascular accident (including transient ischemic attacks) within the 6 months prior to initiation of treatment | 2 | [
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NCT02914171 | 18:36:chronic_disease | Individuals with bleeding disorders | 2 | [
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NCT02122185 | 20:45:treatment,38:45:treatment,,,133:154:treatment,156:163:treatment,168:183:treatment | ubjects undergoing primary debulking surgery must have stage III or IV disease and have undergone surgery to include, at a minimum, removal of the uterus, ovaries and fallopian tubes | 2 | [
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NCT01920737 | 24:39:chronic_disease,90:109:chronic_disease,114:131:chronic_disease | Clinically significant cardiac disease (NY Heart Association Class III or IV), including chronic arrhythmias, or pulmonary disease | 2 | [
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NCT02518594 | 1:31:chronic_disease, | Twin-twin transfusion syndrome, due to increased risk of adverse pregnancy outcome | 2 | [
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NCT02152995 | 48:72:cancer | patients with a history of completely resected non-melanoma skin cancer | 2 | [
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NCT02232516 | 1:33:cancer | Enteropathy-type T-cell lymphoma | 2 | [
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NCT03042767 | 9:39:chronic_disease | Current gastrointestinal (GI) bleeding | 2 | [
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NCT01572480 | 38:60:treatment | Patients who are receiving any other investigational agents | 2 | [
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NCT02446457 | 17:29:treatment | enrolled in the lenalidomide containing cohort (cohort 2) must be registered into the mandatory Revlimid REMS program | 2 | [
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NCT02312518 | 1:20:chronic_disease | sickle cell disease | 2 | [
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NCT02347995 | 1:16:chronic_disease | unstable angina | 2 | [
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NCT02013154 | ,23:29:cancer,115:127:cancer | Must have one or more tumors measurable on radiographic imaging as defined by the Response Evaluation Criteria in Solid Tumors (RECIST). Patients with evaluable but not measurable disease per RECIST criteria may be enrolled with the approval of the medical monitor | 2 | [
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NCT03145298 | 25:47:treatment,, | The subjects must be on PAH-specific therapies for at least 4 months and on a stable dose for at least 4 weeks prior to enrollment into study | 2 | [
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NCT02203552 | 23:39:chronic_disease,43:59:chronic_disease,69:87:cancer | Reported diagnosis of major depression or anxiety disorder prior to breast cancer (BC) diagnosis | 2 | [
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NCT02099591 | 22:33:chronic_disease,37:53:chronic_disease,68:76:chronic_disease | History of prolonged neutropenia or thrombocytopenia with clinical sequelae | 2 | [
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NCT01983462 | 12:35:treatment,39:69:treatment,,128:149:treatment | Use of any investigational product or investigational medical device within 30 days prior to screening, or requirement for any investigational agent prior to completion of all scheduled study assessments | 2 | [
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NCT02560766 | 19:30:chronic_disease,56:79:chronic_disease,90:124:chronic_disease | Positive test for hepatitis B surface antigen (HBsAg), hepatitis C virus (HCV) antibody, human immunodeficiency virus (HIV) antibody at screening | 2 | [
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NCT02806570 | 26:37:chronic_disease,, | Hemodynamic instability: Hypotension (systolic pressure <90 millimeter Mercury (mmHg)) or requirement for inotropic support or mechanical hemodynamic support | 2 | [
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NCT03029884 | 1:18:chronic_disease,,,39:84:chronic_disease,86:117:chronic_disease,119:132:chronic_disease,134:150:chronic_disease,152:187:chronic_disease | Active depression (BDI > 20) or other untreated or uncontrolled psychiatric illness (active general anxiety disorder, schizophrenia, bipolar disorder, obsessive-compulsive disorder (OCD) | 2 | [
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NCT02554253 | 9:24:treatment,17:24:treatment,,89:115:treatment,129:157:treatment | Complex cardiac surgery will be defined as surgery involving more than one heart valve, redo-sternotomy procedures, or combined valvular and CABG procedures | 2 | [
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NCT02163317 | 42:84:treatment, | have a history/physical examination with digital rectal examination of the prostate within 90 days prior to screening | 2 | [
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NCT01941316 | 21:37:chronic_disease,48:57:treatment,59:79:treatment,81:91:treatment,96:107:treatment, | Must not have acute active infection requiring treatment (systemic antibiotics, antivirals, or antifungals) within 14 days prior to enrollment | 2 | [
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NCT02845596 | 7:38:treatment | Prior allogeneic stem cell transplant | 2 | [
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NCT02531295 | 22:44:chronic_disease,83:92:chronic_disease,110:132:chronic_disease,152:178:chronic_disease,195:212:treatment,216:267:treatment,273:291:chronic_disease | Any known history of liver-related diseases including but not limited to: hepatic cirrhosis of decompensated chronic liver diseases; clinically active hepatitis B or C infection as evidenced by clinical jaundice or Grade 2 or higher liver function test abnormalities; any hepatic impairment, regardless of the graded liv... | 2 | [
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NCT01061515 | 62:75:treatment | Appropriate studies will be undertaken in patients receiving HAART therapy, when indicated | 2 | [
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NCT02334865 | 36:56:cancer | Patients with a known diagnosis of plasma cell leukemia | 2 | [
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NCT02404194 | 21:46:chronic_disease | Lifetime history of Axis I psychotic disorder | 2 | [
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NCT02323581 | 20:45:chronic_disease,53:59:chronic_disease,63:84:chronic_disease | Known degenerative connective tissue disease, e.g., Marfan or Ehler-Danlos Syndrome | 2 | [
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NCT02020018 | 1:12:treatment | Thoracotomy | 2 | [
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NCT02393885 | 1:38:chronic_disease,,, | Stroke/cerebrovascular accident (CVA) within previous six months, carotid artery stenosis greater than 80% | 2 | [
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NCT02681614 | 90:106:chronic_disease,108:144:chronic_disease,146:170:chronic_disease,172:190:chronic_disease,195:232:chronic_disease | Patients with 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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NCT01972113 | 21:70:chronic_disease | Subjects presenting chronic degenerative and/or inflammatory diseases | 2 | [
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NCT01028846 | 28:50:chronic_disease,62:72:treatment,74:130:treatment,132:146:treatment,151:159:treatment | Medications for medical or psychiatric conditions including: dofetilide, fosphenytoin/phenytoin trichlormethiazide (any thiazide), chlorpromazine and warfarin | 2 | [
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NCT02582827 | 18:25:chronic_disease,29:40:chronic_disease,136:143:treatment | Any uncontrolled medical or psychiatric risk factors that would contraindicate the use or impair the ability of the patient to receive therapy per protocol or that may impose excessive risk to the patient | 2 | [
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NCT02311361 | 1:9:chronic_disease | Dementia or significantly altered mental status that would prohibit the understanding or rendering of Information and Consent and compliance with the requirements of the protocol | 2 | [
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NCT02744430 | 27:61:treatment | Patients already taking a beta-adrenergic agonist medication | 2 | [
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NCT02155699 | 25:50:chronic_disease | meeting criteria for an Axis I psychotic disorder | 2 | [
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NCT02232516 | ,,83:105:treatment | with a cumulative illness rating scale (CIRS) score >= 6 OR deemed ineligible for cytotoxic chemotherapy by the treating investigator | 2 | [
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NCT02734134 | 48:62:treatment,64:80:treatment,85:117:treatment | Resistant organisms not sensitive to available IV antibiotics, oral antibiotics, or heat stable antibiotic additives to bone cement with documented elution characteristics | 2 | [
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NCT02833805 | 14:23:chronic_disease,25:30:chronic_disease,35:51:chronic_disease | Uncontrolled bacterial, viral, or fungal infection | 2 | [
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NCT03043742 | 11:24:chronic_disease | End stage renal disease | 2 | [
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NCT02245997 | 41:62:chronic_disease | Patients with any concurrent medical or psychiatric condition or disease which, in the investigator's judgment, would make them inappropriate candidates for entry into this study | 2 | [
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NCT02576301 | 16:34:chronic_disease | Any history of hemorrhagic stroke | 2 | [
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NCT03162731 | 1:24:cancer | squamous cell carcinoma of the skin | 2 | [
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NCT02131597 | 5:17:treatment,10:17:treatment,,134:153:chronic_disease | Off chemotherapy for 2 weeks prior to entering this study with no toxic effects of that therapy, unless there is evidence of rapidly progressive disease | 2 | [
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NCT02805504 | 21:37:treatment | Patients undergoing urologic surgery | 2 | [
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NCT02464436 | 15:25:cancer,34:58:cancer,60:84:cancer,89:103:cancer | No history of malignancy, except non-melanoma skin cancer; pre-malignant conditions and cancer in situ | 2 | [
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NCT02440581 | ,85:100:treatment,105:117:treatment,145:155:treatment,157:174:treatment,182:195:treatment | Treatment within last 6 months with drugs that may affect bone metabolism including bisphosphonates and teriparatide (except for treatment with calcitriol, vitamin D analogs and/or calcimimetics) | 2 | [
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NCT01878617 | ,,,,141:160:cancer | ≥5 years at the time of remediation intervention consent or age is greater than or equal to 22 years and less than 40 years and patient has SHH medulloblastoma | 2 | [
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