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NCT02159495 | 41:48:chronic_disease,,,, | ONLY research participants experiencing hypoxia with oxygen saturation less than 92% are required to have diffusion capacity of carbon monoxide (DLCO) or forced expiratory volume in one second (FEV1) > 45% predicted | 1 | [
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NCT02269293 | 15:33:cancer,37:63:cancer,78:90:treatment,78:96:treatment,113:139:treatment,257:281:treatment,369:389:treatment,448:457:cancer | Patients with endometrial cancer or endometrial carcinosarcoma may either be chemotherapy naive OR have had one prior line of chemotherapy that must have been a platinum-based chemotherapy regimen in the adjuvant or advanced/recurrent setting. The initial platinum-based treatment may have included consolidation/maintenance and/or biologic/targeted agents as part of first-line treatment. Patients entering the trial chemotherapy naive MUST have Stage IVB or recurrent disease AND have disease that is not amenable to curative intent | 1 | [
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NCT03043794 | 1:26:cancer | Invasive ductal carcinoma | 1 | [
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NCT02146924 | 39:52:treatment,146:177:treatment,189:229:treatment | If research participant is undergoing leukapheresis and the research participant has undergone prior alloSCT, two months must have elapsed since allogeneic stem cell transplant to undergo PBMC collection for T cell manufacturing | 1 | [
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NCT02530463 | 5:18:treatment,20:32:treatment,34:46:treatment,48:64:treatment,66:79:treatment,81:101:treatment,,130:159:treatment | Any major surgery, radiotherapy, chemotherapy, biologic therapy, immunotherapy, experimental therapy within 2 weeks prior to the first dose of the study drugs | 1 | [
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NCT02234934 | 1:7:chronic_disease,, | Anemia (hemoglobin < 8 g/dl) | 1 | [
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NCT02512926 | ,,,64:83:treatment | ANC ≥ 750 - cannot be transfused (must be ≥ 72 hours from last neutrophil infusion) | 1 | [
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NCT02464878 | 1:21:chronic_disease,23:37:chronic_disease,43:70:chronic_disease | Invasive aspergillus, histoplasmosis, and coccidoidomycosis infection within the last year | 1 | [
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NCT01130077 | 28:35:cancer,41:59:cancer,85:115:treatment,98:107:treatment,108:115:treatment,155:167:treatment | Newly diagnosed high-grade gliomas with metastatic disease within the CNS requiring craniospinal radiation therapy. Patients may or may not have received chemotherapy during radiation, but cannot have received chemotherapy after radiation therapy was completed | 1 | [
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NCT02501473 | 1:62:treatment | Prior administration of other intratumoral immunotherapeutics | 1 | [
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NCT02268448 | 8:16:treatment, | Use of nicotine-containing products for the past 6 months prior to study start | 1 | [
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NCT03096288 | 51:61:allergy_name | History of a serious hypersensitivity reaction to evolocumab | 1 | [
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NCT02124772 | 19:31:cancer,53:88:cancer,108:131:cancer,171:185:cancer,189:205:cancer,209:232:chronic_disease | For subjects with solid tumors that are not primary central nervous system (CNS) tumors or NF-1 associated plexiform neurofibromas subjects with symptomatic or untreated leptomeningeal or brain metastases or spinal cord compression | 1 | [
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NCT02003222 | 64:74:treatment | Patients must be considered reliable enough to comply with the medication regimen and follow-up, and have social support necessary to allow this compliance | 1 | [
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NCT02755116 | 1:22:chronic_disease | Narrow angle glaucoma | 1 | [
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NCT02577406 | 1:32:cancer | Carcinoma in situ of the cervix | 1 | [
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NCT03176784 | 56:75:treatment | desire to quit smoking but not be engaged currently in cessation treatment | 1 | [
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NCT02347891 | 1:10:chronic_disease | Hepatitis status will be obtained from patients' medical records | 1 | [
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NCT01793519 | 26:40:treatment | Unwilling to discontinue anti-TNF agent | 1 | [
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NCT02210078 | 36:46:cancer | Active and uncontrolled relapse of malignancy | 1 | [
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NCT02451553 | ,15:92:treatment | #ERROR! | 1 | [
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NCT01999179 | 9:20:chronic_disease | Current hematologic | 1 | [
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NCT02400554 | ,19:38:chronic_disease | Women who exhibit serious psychiatric symptoms determined by CNO trained staff | 1 | [
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NCT02479230 | 9:18:treatment | Current treatment on another clinical trial | 1 | [
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NCT02468024 | 39:65:cancer, | Radiographic findings consistent with non-small cell lung cancer, including lesions with ground glass opacities with a solid component of 50% or greater | 1 | [
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NCT01660607 | 79:89:treatment | Psychosocial circumstances that preclude the patient being able to go through transplant or participate responsibly in follow up care | 1 | [
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NCT01869114 | 1:10:treatment,17:25:treatment,27:34:treatment,36:43:treatment | Verapamil (e.g. Calan SR, Isoptin, Verelan) | 1 | [
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NCT02762266 | 1:30:chronic_disease, | Active gastrointestinal bleed within 2 weeks of study enrollment | 1 | [
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NCT02332928 | 1:14:chronic_disease,, | hypercalcemia (calcium >11 mg/dL) Ca = SerumCa + 0.8 * (NormalAlbumin - PatientAlbumin) | 1 | [
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NCT02259621 | 1:26:cancer,28:43:cancer,45:52:cancer,54:60:cancer,62:67:cancer,71:97:cancer | non melanoma skin cancers, in situ bladder, gastric, breast, colon or cervical cancers/dysplasia | 1 | [
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NCT02950337 | 18:29:cancer | Prior history of lung cancer | 1 | [
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NCT02507505 | 1:23:treatment | total hip arthroplasty | 1 | [
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NCT02132130 | 104:107:treatment | Immunocompromised patients, as judged by the investigators based on patient history, physical exam and CBC | 1 | [
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NCT02479620 | 8:27:treatment,34:51:treatment,68:90:treatment,106:131:treatment,135:200:treatment, | Use of alternative therapy, e.g. radiation therapy, as part of the index lesion treatment, or use of any drug eluting stents (DES) or drug-eluting balloon/drug-coated balloons (DEB/DCB) for treatment of any infra-inguinal lesions during the study procedure or during the initial six-month follow up period | 1 | [
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NCT01701986 | 21:30:chronic_disease,32:37:chronic_disease,41:58:chronic_disease | Active uncontrolled bacterial, viral or fungal infections | 1 | [
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NCT02549937 | 10:35:treatment,39:61:treatment,,90:128:treatment | Received investigational treatment in another clinical study within 4 weeks prior to the initiation of investigational treatmen | 1 | [
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NCT02341963 | 46:54:treatment | the inability to avoid these products during ketamine administration | 1 | [
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NCT02425566 | 1:9:chronic_disease | diabetes | 1 | [
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NCT02061553 | 52:65:treatment | Concurrent involvement in one-to-one counseling or psychotherapy for emotional issues | 1 | [
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NCT00715611 | 1:18:treatment | Prior nephrectomy on the contralateral side of MPM | 1 | [
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NCT00788164 | 4:28:treatment, | No investigational agent(s) within the past 6 months | 1 | [
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NCT03157713 | 1:34:chronic_disease | Chronic Kidney Disease stage IV/V | 1 | [
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NCT02387905 | 21:43:treatment | Patients undergoing bisphosphonate therapy | 1 | [
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NCT02723994 | 1:14:cancer | CNS3 leukemia | 1 | [
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NCT01037790 | 45:79:chronic_disease | The subject is known to be positive for the human immunodeficiency virus (HIV) | 1 | [
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NCT01730118 | ,,,,,,,212:225:treatment | Willingness of female and male subjects to use effective contraception e.g. oral contraceptives, barrier device, intrauterine device, or condoms, during the study and for three months following the last dose of study vaccine | 1 | [
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NCT03029884 | 1:22:chronic_disease,29:58:chronic_disease,60:91:chronic_disease,108:135:chronic_disease | personality disorders (e.g. multiple personality disorder, borderline personality disorder, etc.) or other neuropsychiatric conditions that evaluating psychiatrist would recommend exclusion of patient after neuropsychiatric evaluation | 1 | [
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NCT01512888 | 43:69:treatment | Availability of a HLA matched sibling for allogeneic transplantation | 1 | [
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NCT02334865 | 34:49:chronic_disease,55:89:chronic_disease,91:114:chronic_disease,118:141:chronic_disease | Known seropositive for or active viral infection with human immunodeficiency virus (HIV), hepatitis B virus (HBV) or hepatitis C virus (HCV) | 1 | [
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NCT02907983 | ,75:90:treatment,98:113:treatment,117:127:treatment | post-menopausal women whose vasomotor symptoms are refractory to approved oral treatments (i.e., hormone therapy or paroxetine) | 1 | [
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NCT02270619 | 7:23:chronic_disease | other chronic diseases | 1 | [
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NCT03179163 | 1:16:chronic_disease | kidney problems | 1 | [
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NCT02498613 | 77:93:chronic_disease,107:131:chronic_disease,133:157:chronic_disease,159:177:chronic_disease,182:219:chronic_disease | 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 | 1 | [
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NCT00930228 | 25:33:chronic_disease | A previous diagnosis of diabetes | 1 | [
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NCT02678910 | 21:54:cancer | Participants with a large cancerous mass in the ovary that is being removed; cryopreservation will not be performed on portions of the ovary | 1 | [
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NCT02362997 | 102:115:allergy_name | History of allergic reactions attributed to compounds of similar chemical or biologic composition to pembrolizumab | 1 | [
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NCT02554383 | 7:27:chronic_disease,35:44:chronic_disease,46:64:chronic_disease,66:91:chronic_disease | Other concurrent infection (e.g., pneumonia, acute otitis media, streptococcal pharyngitis) | 1 | [
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NCT02257138 | 85:98:treatment,116:138:treatment | patients with newly diagnosed or previously treated disease are eligible as long as prior therapy does not include hypomethylating agents | 1 | [
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NCT02404194 | 21:44:chronic_disease,59:72:chronic_disease,82:88:chronic_disease,92:108:chronic_disease | clear evidence that psychosis-risk syndrome is due to non-schizophrenia-spectrum Axis I or Axis II disorder | 1 | [
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NCT02111824 | ,,92:129:treatment | subjects with peripheral lung lesions that are <1.5 cm in size who are planning to undergo percutaneous image guided lung biopsy as part of their routine medical care | 1 | [
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NCT02395614 | 11:25:treatment | bilateral reconstruction using other techniques | 1 | [
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NCT02823665 | 1:18:chronic_disease | Myasthenia gravis | 1 | [
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NCT01174121 | 24:42:chronic_disease | History of major organ autoimmune disease | 1 | [
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NCT02132598 | 54:70:chronic_disease,84:93:treatment,97:135:treatment | Patients must have received at least one regimen for systemic disease which may be cytotoxic or oral tyrosine kinase inhibitor therapy | 1 | [
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NCT02592551 | 12:41:cancer | History of leptomeningeal carcinomatosis | 1 | [
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NCT01807091 | 51:63:chronic_disease,65:74:chronic_disease,76:92:chronic_disease | Afebrile with clear chest imaging and no signs of active viral, bacterial, fungal infection unless determined to be, at the discretion of the investigator, not clinically significant in the context of this study | 1 | [
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NCT03059888 | 26:38:treatment, | Subject has received any live vaccine within 3 months of screening | 1 | [
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NCT02503358 | 21:30:treatment | Conception while on treatment must be avoided | 1 | [
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NCT02891447 | 1:29:cancer | Positive peritoneal cytology | 1 | [
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NCT03153319 | 22:29:treatment | Requirement for live vaccine exposure that would be expected to occur during the time frame of the study | 1 | [
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NCT02664909 | 6:23:chronic_disease | with coronary ischemia | 1 | [
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NCT02094794 | 57:79:treatment,107:119:treatment,124:141:treatment | Plans during the trial to receive any other (non-trial) investigational agents, or concurrent biological, chemotherapy, or radiation therapy | 1 | [
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