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NCT02013492 | 27:39:chronic_disease,,,, | Patients with significant lung disease, an ejection fraction less than 40%, or a resting heart rate less than 60/min will not be enrolled | 2 | [
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NCT02336217 | 1:10:treatment | Treatment by Marshall Internal Medicine Department | 2 | [
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NCT02133573 | ,,,,110:130:treatment | History of preterm birth or short cervix (defined as cervical length ≤ 25 mm at 18-24 weeks GA necessitating progesterone therapy | 2 | [
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NCT02530073 | ,,77:109:treatment | Preterm labor, cervix shortened (<15 mm at enrollment or within 24 hours of FETO balloon insertion procedure) or uterine anomaly strongly predisposing to preterm labor, placenta previa | 2 | [
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NCT03100435 | 36:57:allergy_name,67:104:chronic_disease,108:126:chronic_disease | Subjects with contraindications to wearing a mouth guard, such as chronic obstructive pulmonary disease or severe sleep apnea | 2 | [
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NCT02581787 | 21:39:treatment,30:39:treatment,41:53:treatment,55:71:treatment,76:89:treatment | No prior receipt of systemic treatment (chemotherapy, targeted therapy, or immunotherapy) for the lesion under consideration of treatment | 2 | [
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NCT01891812 | 15:34:chronic_disease | Patients with sickle cell disease | 2 | [
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NCT00788164 | 15:51:cancer | No concurrent adenocarcinoma in situ of the cervix | 2 | [
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NCT02446457 | 17:29:treatment, | enrolled in the lenalidomide cohort must adhere to the scheduled pregnancy testing as required in the Revlimid Risk Evaluation and Mitigation Strategy (REMS) program | 2 | [
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NCT02471430 | 27:37:chronic_disease | No clinically significant eye disease | 2 | [
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NCT02964039 | 17:23:chronic_disease | Experience of a stroke 6 months prior to participation | 2 | [
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NCT03153969 | 12:32:chronic_disease | Teeth with periapical pathology | 2 | [
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NCT02105545 | 20:29:cancer | Any patient with a malignant diagnosis at the time of diagnosis or relapse | 2 | [
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NCT02169739 | 33:64:chronic_disease | other prior cortical or retinal transient ischemic attack (TIA) | 2 | [
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NCT01459107 | 119:137:treatment,244:253:treatment,356:387:treatment | No co-existing medical condition which, in the opinion of the study team, could affect the immunomodulatory protocol, surgical procedure, or functional results (see Donor and Recipient Exclusion Criteria below. If the condition is amenable to treatment, the study team must agree that said condition should not significa... | 2 | [
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NCT01220583 | 4:31:treatment,35:52:treatment,57:82:cancer,84:102:treatment,119:125:cancer | No prior systemic chemotherapy or radiation therapy for salivary gland malignancy (prior chemotherapy for a different cancer is allowable) | 2 | [
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NCT03029806 | 15:27:chronic_disease,29:37:chronic_disease,39:45:chronic_disease,47:70:chronic_disease,72:86:chronic_disease,88:94:cancer,96:111:chronic_disease,113:125:chronic_disease,130:146:treatment, | No history of hypertension, diabetes, stroke, coronary artery disease, kidney disease, cancer, thyroid disease, preeclampsia, or hospitalizations in 6 months | 2 | [
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NCT02978638 | 21:36:chronic_disease | Active or recurrent pressure ulcers, particularly in sacral, ischial or trochanteric areas | 2 | [
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NCT02583893 | 22:32:cancer,,,104:120:cancer,133:147:cancer,152:169:cancer | Previously untreated non-M3 AML age >60 with no evidence of favorable karyotype defined by presence of t(8;21)(q22;q22) [AML1-ETO], inv16(p13;q22), or t(16;16)(p13;q22) [CBFβ;MYH11] by cytogenetics, FISH, or RT-PCR | 2 | [
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NCT02013154 | 31:49:chronic_disease,82:90:chronic_disease,92:109:chronic_disease,114:123:chronic_disease,138:156:treatment | History of known or suspected autoimmune disease with the specific exceptions of vitiligo, atopic dermatitis, or psoriasis not requiring systemic treatment | 2 | [
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NCT02710396 | 1:12:chronic_disease, | Hepatitis C (e.g., HCV RNA [qualitative] is detected) | 2 | [
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NCT02617589 | 24:27:cancer | Recurrent or secondary GBM | 2 | [
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NCT03104699 | 1:14:treatment,24:98:treatment,107:116:treatment,118:128:treatment,133:190:treatment | Prior therapy with any antibody/drug targeting T-cell co-regulatory proteins (immune checkpoints) such as anti-PD-1, anti-PD-L1, or anti-cytotoxic T-lymphocyte antigen 4 (CTLA-4) antibodies | 2 | [
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NCT02543983 | 87:99:chronic_disease,101:109:chronic_disease,133:144:treatment | Presence of medical illness likely to alter brain morphology and/or physiology (e.g., hypertension, diabetes) even if controlled by medications | 2 | [
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NCT02780401 | 15:29:cancer,31:44:cancer,46:73:cancer | Patients with non-metastatic, node positive, HER2 negative breast cancer, confirmed by pathology report, who are in remission and defined as having no evidence of disease (NED) | 2 | [
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NCT00630565 | 15:40:chronic_disease,75:82:cancer,84:92:cancer,127:142:treatment | Patients with cytogenetic abnormalities suggesting an improved prognosis [t(8:21), t(15;17) and inv(16)] will be eligible for transplantation in first remission | 2 | [
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NCT02339922 | 51:73:treatment, | Participation in other clinical trials with other investigational agents not included in this trial, within 21 days of the start of this trial and throughout the duration of this trial | 2 | [
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NCT02369653 | 1:33:chronic_disease | Uncontrolled severe hypertension at enrollment | 2 | [
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NCT01600131 | 56:62:chronic_disease | All caregivers of Veterans with a primary diagnosis of stroke | 2 | [
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NCT02053909 | 12:35:chronic_disease | History of intracranial hemorrhage | 2 | [
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NCT00001337 | 1:31:cancer | mediastinal gray zone lymphoma | 2 | [
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NCT01943851 | ,,,,127:138:treatment | In addition, male subjects whose partners are or become pregnant must continue to use condoms for 7 days after stopping study medications | 2 | [
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NCT03043807 | 1:16:treatment, | hormone therapy was recently initiated (<90 days duration)) | 2 | [
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NCT02468024 | 15:46:cancer | Patients with non-peripheral (central) tumors are NOT eligible | 2 | [
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NCT02356653 | 1:10:cancer | Lymphomas | 2 | [
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NCT02675959 | 56:75:chronic_disease | Patients must demonstrate one or more of the following Sickle Cell Disease Complications (or patients in Cohort 2 can meet other high risk criteria instead) | 2 | [
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NCT01894061 | 16:27:treatment | The effects of bevacizumab on developing fetus or nursing infant are not known | 2 | [
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NCT01799538 | 47:68:cancer,70:87:cancer,89:109:chronic_disease | evidence of lung and other organ involvement (renal angiomyolipomas, chylous effusions, lymphangioleiomyomas) | 2 | [
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NCT02213913 | 1:16:cancer,22:62:treatment,36:56:treatment,209:213:cancer,216:219:cancer,245:257:treatment | B-cell lymphoma with comprehensive immunohistochemistry (IHC) panel establishing lineage (CD20, CD3) and cell of origin (CD10, BCL6 and MUM1) in addition to proliferative/prognostic markers (Ki-67, C-myc and BCL2). DHL will be identified using cytogenetics and/or immunohistochemistry | 2 | [
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NCT01943851 | 8:22:treatment,30:38:treatment,40:47:treatment,, | Use of anticoagulants (e.g., warfarin, heparin) at therapeutic levels within 7 days prior to the first dose of GSK525762 | 2 | [
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NCT03070535 | 27:33:cancer | Remote history of treated cancer is ok, as long as current cognition and digestion are not affected | 2 | [
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NCT01928589 | 38:75:treatment,77:85:treatment,87:125:treatment,127:161:treatment,176:215:treatment,255:267:treatment,269:285:treatment,289:300:treatment,460:486:treatment,,,546:561:treatment,,,,,721:737:treatment,,839:856:treatment | Recommended regimens are as follows: Cyclophosphamide and Doxorubicin (AC); Taxotere, Doxorubicin and Cyclophosphamide (TAC); Taxotere and Cyclophosphamide (TC); or Taxotere, Carboplatin and Trastuzamab (TCH) prior to registration. The use of additional chemotherapy, hormonal therapy or Trastuzumab after the initial re... | 2 | [
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NCT01925131 | 111:118:treatment,,,210:222:treatment,224:246:treatment,250:274:treatment | in addition to routine contraceptive methods, effective contraception also includes heterosexual celibacy and surgery intended to prevent pregnancy (or with a side-effect of pregnancy prevention) defined as a hysterectomy, bilateral oophorectomy or bilateral tubal ligation | 2 | [
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NCT02033941 | 1:21:chronic_disease,32:51:chronic_disease,53:69:chronic_disease,74:98:chronic_disease, | Major mental illness including psychotic disorders, bipolar disorder, or major depressive episode that is not in remission for less than 12 months | 2 | [
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NCT01994382 | ,,70:73:cancer,74:77:cancer,81:108:cancer,110:115:cancer,117:119:cancer,121:124:cancer,126:129:cancer,131:157:cancer | Specific Patient at least 18yrs of age with histologically confirmed CLL/SLL or B-cell Non-Hodgkin lymphoma (DLBCL, FL, MCL, MZL, lymphoplasmacytic lymphoma) | 2 | [
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NCT02570854 | 1:18:treatment, | Blood transfusion administered within 4 weeks prior to baseline | 2 | [
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NCT01659541 | 1:10:chronic_disease,12:32:chronic_disease,37:51:chronic_disease | Scoliosis, chest wall deformity, or marked obesity | 2 | [
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NCT02876302 | 43:61:cancer | Extensive nodal involvement is defined as metastatic disease involving any nodal region outside of the involved breast | 2 | [
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NCT01624090 | 63:75:cancer,80:101:cancer,103:119:cancer,121:137:cancer,139:170:cancer,174:193:cancer | Patients with measurable inoperable, histologically confirmed primary lung and esophageal carcinomas, thymic neoplasms, germ cell tumors, malignant pleural mesotheliomas or chest wall sarcomas | 2 | [
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NCT02315196 | 13:29:chronic_disease,37:52:chronic_disease,54:71:chronic_disease | Significant vascular disease (e.g., aortic aneurysm, aortic dissection) | 2 | [
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NCT03063892 | 12:35:chronic_disease | History of intracranial hemorrhage | 2 | [
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NCT01627301 | 63:67:chronic_disease | Prehypertensive and Normotensive OEF/OIF/OND veterans without PTSD (controls) | 2 | [
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NCT02973425 | 60:76:treatment,, | The Food and Drug Administration (FDA) advises caution for nicotine lozenge use among women who are pregnant | 2 | [
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NCT03059355 | 1:24:cancer | squamous cell carcinoma | 2 | [
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NCT02121158 | ,,,23:36:chronic_disease | NYHA Class II and III heart failure | 2 | [
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NCT03049189 | 9:28:treatment | Planned alternative therapy (for the period of study participation) | 2 | [
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NCT02857270 | 83:89:treatment | Currently using concomitant medications that are strong inhibitors or inducers of CYP3A4 | 2 | [
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NCT02484404 | ,19:60:treatment | with at least one prior line of platinum-based chemotherapy are eligible | 2 | [
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NCT01947140 | 1:17:cancer | Multiple Myeloma patients specified in the protocol | 2 | [
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NCT02253316 | 1:17:cancer | multiple myeloma | 2 | [
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NCT02234193 | 22:53:treatment | scheduled to undergo elective abdominoplasty surgery at MGH | 2 | [
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NCT02128802 | 21:29:treatment | Non-compliance with dialysis regimen | 2 | [
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