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NCT01620216 | 7:41:chronic_disease | Known human immunodeficiency virus (HIV)-positive patient | 1 | [
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NCT01415882 | 7:41:chronic_disease | Known human immunodeficiency virus (HIV) positive | 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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NCT00716066 | 45:79:chronic_disease | Patients who are serologically positive for human immunodeficiency virus (HIV) | 1 | [
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NCT03135171 | 10:27:treatment, | The last radiation therapy must have occurred ≥3 weeks prior to study registration | 1 | [
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NCT03113825 | 7:24:treatment | Prior radiation therapy to the chest [Period 2] | 1 | [
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NCT03077243 | 18:35:treatment | Prior history of radiation therapy to the head and neck | 1 | [
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NCT03076333 | 40:57:treatment | Previous radiation exposure precluding radiation therapy | 1 | [
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NCT02982226 | 12:29:treatment | History of radiation therapy of the affected foot | 1 | [
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NCT02774421 | 37:54:treatment | Patients who have already undergone radiation therapy for current recurrence | 1 | [
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NCT02501473 | 20:37:treatment | For Parts 4 and 5, radiation therapy is omitted | 1 | [
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NCT02496208 | 26:43:treatment | The subject has received radiation therapy | 1 | [
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NCT02442635 | 11:28:treatment | Receiving radiation therapy | 1 | [
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NCT02434809 | 32:49:treatment | Patient is planning to undergo radiation therapy for primary | 1 | [
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NCT02315612 | 1:18:treatment, | radiation therapy 3 weeks prior to apheresis | 1 | [
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NCT02291848 | ,,72:89:treatment | Pulse oximetry of >93% on room air in patients who previously received radiation therapy | 1 | [
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NCT02277548 | 33:50:treatment | Patients anticipated to receive radiation therapy with Protons | 1 | [
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NCT02236013 | 13:30:treatment, | Subject has radiation therapy within 4 weeks prior to the first study dose | 1 | [
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NCT02217709 | 50:67:treatment | Patients should not be considered candidates for radiation therapy | 1 | [
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NCT02208362 | ,123:140:treatment | Radiographic evidence of progression/recurrence of the measurable disease more than 12 weeks after the end of the initial radiation therapy | 1 | [
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NCT02163317 | ,,139:156:treatment | willing and able to complete the Expanded Prostate Cancer Index Composite (EPIC) questionnaire (baseline, 6, 12 and 24 months post end of radiation therapy) | 1 | [
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NCT02160288 | 10:27:treatment | Previous radiation therapy to the anal canal and rectum | 1 | [
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NCT02132598 | 26:43:treatment | The subject has received radiation therapy | 1 | [
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NCT02125786 | 32:49:treatment, | Interval from start of initial radiation therapy to enrollment > 9 months | 1 | [
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NCT02125786 | ,,67:84:treatment | Pregnant women are excluded from enrollment on this study because radiation therapy is an agent with the potential for teratogenic or abortifacient effects | 1 | [
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NCT02112617 | 83:100:treatment | Participants or their legal guardian must sign consent prior to the initiation of radiation therapy | 1 | [
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NCT02112617 | 54:71:treatment, | Patients will be ineligible if any prior therapeutic radiation therapy > 500 cGy has been delivered | 1 | [
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NCT02112617 | ,,,99:116:treatment | Women of childbearing age/menstruating must have a negative pregnancy test prior to initiation of radiation therapy | 1 | [
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NCT02110992 | 31:48:treatment | Original pathology report and radiation therapy records not available | 1 | [
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NCT02078102 | 33:50:treatment, | Patients must not have received radiation therapy within the past 4 weeks | 1 | [
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NCT01992861 | 24:41:treatment | Patients with no prior radiation therapy to the pelvis | 1 | [
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NCT01941316 | 37:54:treatment, | Patients may have received previous radiation therapy, but it must have been completed at least 21 days prior to enrollment and the patient should have recovered from all associated toxicities | 1 | [
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NCT01878617 | 29:46:treatment | Completed protocol-directed radiation therapy | 1 | [
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NCT01871766 | 30:47:treatment | Patients requiring emergency radiation therapy are eligible for enrollment on this study | 1 | [
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NCT01817751 | ,43:60:treatment, | At least 12 weeks since the completion of radiation therapy to a total of >=50Gy | 1 | [
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NCT01659203 | 27:44:allergy_name | History of sensitivity to radiation therapy | 1 | [
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NCT01333046 | ,,88:105:treatment | Pulse oximetry of more than 95 percent on room air in patients who previously received radiation therapy | 1 | [
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NCT03138512 | 35:53:chronic_disease | with an active known or suspected autoimmune disease | 1 | [
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NCT03123783 | 28:46:chronic_disease | Active, known or suspected autoimmune disease | 1 | [
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NCT03104699 | 26:44:chronic_disease | Active or history of any autoimmune disease | 1 | [
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NCT03001882 | 46:64:chronic_disease | Participants with active, known or suspected autoimmune disease | 1 | [
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NCT02988960 | 57:75:chronic_disease, | Participant must not have an active or prior documented autoimmune disease in the last 2 years | 1 | [
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NCT02955251 | 28:46:chronic_disease, | Active or prior documented autoimmune disease in the last 2 years | 1 | [
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NCT02947165 | 42:60:chronic_disease | Patients with active, known or suspected autoimmune disease | 1 | [
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NCT02912572 | 8:26:chronic_disease | Active autoimmune disease that might deteriorate when receiving an immunostimulatory agent | 1 | [
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NCT02910700 | 98:116:chronic_disease | inhaled or topical steroids and adrenal replacement doses are permitted in the absence of active autoimmune disease | 1 | [
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NCT02762006 | 28:46:chronic_disease, | Active or prior documented autoimmune disease within the past 2 years | 1 | [
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NCT02553642 | 22:40:chronic_disease | Subjects with active autoimmune disease, symptoms or conditions | 1 | [
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NCT02536794 | 38:56:chronic_disease | Patients with a history of or active autoimmune disease | 1 | [
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NCT02520791 | 43:61:chronic_disease | Patients with active, known, or suspected autoimmune disease | 1 | [
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NCT02519322 | 42:60:chronic_disease | Subjects with active, known or suspected autoimmune disease | 1 | [
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NCT02502708 | 8:26:chronic_disease | Active autoimmune disease | 1 | [
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NCT02477826 | 45:63:chronic_disease | Subjects with an active, known or suspected autoimmune disease | 1 | [
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NCT02454010 | 1:19:chronic_disease | autoimmune disease | 1 | [
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NCT02452268 | 12:30:chronic_disease | History of autoimmune disease | 1 | [
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NCT02439450 | 28:46:chronic_disease | Active, known or suspected autoimmune disease | 1 | [
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NCT02419495 | 45:63:chronic_disease | subjects with an active, known or suspected autoimmune disease | 1 | [
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NCT02401074 | 1:19:chronic_disease | autoimmune disease | 1 | [
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NCT02350764 | 45:63:chronic_disease | Patients with known or suspected history of autoimmune disease | 1 | [
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NCT02323126 | 53:71:chronic_disease | any known or suspected, current or past history of, autoimmune disease | 1 | [
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NCT02259621 | 66:84:chronic_disease | Subjects are excluded if they have an active, known or suspected autoimmune disease | 1 | [
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NCT01928576 | 31:49:chronic_disease | Any active history of a known autoimmune disease | 1 | [
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NCT01174121 | 24:42:chronic_disease | History of major organ autoimmune disease | 1 | [
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NCT03169543 | 9:19:chronic_disease | Current depression as assessed on the HDRS-17 (for depressed group only) | 1 | [
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NCT03107039 | 14:24:chronic_disease | Experiencing depression symptoms and generally healthy | 1 | [
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NCT03088592 | 47:57:chronic_disease,, | Currently uncontrolled clinically significant depression (BDI>20) | 1 | [
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NCT03034564 | 19:29:chronic_disease | Poorly controlled depression | 1 | [
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NCT02979327 | 1:11:chronic_disease | depression | 1 | [
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NCT02964182 | 30:40:chronic_disease | Certain medications to treat depression | 1 | [
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NCT02880215 | 21:31:chronic_disease | moderate or greater depression symptoms | 1 | [
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NCT02809677 | 9:19:chronic_disease | current depression secondary to substances or general medical condition | 1 | [
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NCT02721537 | 12:22:chronic_disease | History of depression preceding a concussion | 1 | [
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NCT02674529 | 22:32:chronic_disease | history of resistant depression | 1 | [
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NCT02627495 | 23:33:chronic_disease,, | Suffering from severe depression (as defined by a score of >30 in the Beck Depression Inventory) | 1 | [
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NCT02615353 | 11:21:chronic_disease | Diagnosed depression or other condition that may impact QoL | 1 | [
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NCT02570672 | 11:21:chronic_disease,, | Untreated depression or Geriatric Depression Scale score on 15-item scale >7 | 1 | [
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NCT02565199 | 9:19:chronic_disease,, | Current depression (score more than 7 on the Hamilton Depression Rating Scale (HDRS)) | 1 | [
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NCT02466126 | 46:56:chronic_disease | must have clinically significant symptoms of depression | 1 | [
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NCT02440815 | 22:32:chronic_disease | Moderate severity of depression using the Hamilton Depression Rating Scale | 1 | [
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NCT02339233 | 27:37:chronic_disease | no clinically significant depression | 1 | [
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NCT02230605 | 8:18:chronic_disease,, | Active depression as indicated by Geriatric Depression Scale screening test (score ≥ 10) | 1 | [
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NCT02131467 | 8:18:chronic_disease | Active depression | 1 | [
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NCT02104349 | 15:25:chronic_disease | Patients with depression (established during the screening questionnaire) | 1 | [
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NCT02013492 | 25:35:chronic_disease | Patients with worsening depression that has not been addressed clinically | 1 | [
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NCT01948739 | 11:21:chronic_disease | Untreated depression that may affect motivation to participate in the study | 1 | [
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NCT01770587 | 14:24:chronic_disease | Diagnosis of depression | 1 | [
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NCT01742182 | 13:23:chronic_disease,, | Presence of depression defined as the Beck Depression Inventory (BDI) score >14 | 1 | [
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NCT01614990 | 8:18:chronic_disease | Severe depression as determined by the investigator | 1 | [
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