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NCT02509507 | 16:30:treatment,113:123:cancer,128:148:treatment | expected other cancer therapy while on study with the exception of local radiation to the site of bone or other metastasis for palliative treatment | 2 | [
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NCT02414269 | 1:13:treatment,15:31:treatment,43:68:treatment,73:85:treatment, | Chemotherapy, targeted therapy (such as a tyrosine kinase inhibitor) or radiotherapy must have been completed at least 14 days prior to administration of T cells | 2 | [
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NCT01449149 | 27:35:cancer | other soft tissue or bony sarcomas | 2 | [
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NCT01951885 | 27:34:chronic_disease,49:68:chronic_disease,156:163:treatment | Patients with any medical illness or concurrent psychiatric illness which, in the investigators' opinion, cannot be adequately controlled with appropriate therapy | 2 | [
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NCT02000115 | 31:48:cancer,50:58:chronic_disease,62:72:chronic_disease | Echocardiographic evidence of intracardiac mass, thrombus or vegetation | 2 | [
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NCT02020707 | 45:72:cancer | histologic proof of surgically unresectable stage IV malignant melanoma | 2 | [
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NCT03016130 | 17:26:chronic_disease | Untreated major infection at presentation | 2 | [
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NCT01967849 | 19:43:chronic_disease | family history of type 2 diabetes mellitus | 2 | [
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NCT01054196 | 82:97:treatment | Patients must have an adequate number of CD34+ stem cells collected to allow for transplantation | 2 | [
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NCT02382549 | 22:29:treatment,32:39:treatment,42:50:treatment | Growth factors (e.g. Procrit®, Aranesp®, Neulasta®) | 2 | [
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NCT02525861 | 43:53:cancer,,176:186:cancer,190:225:cancer,227:258:cancer,270:285:cancer,300:309:treatment | The participant is experiencing an active malignancy or has a history of malignancy within 5 years prior to screening, with the exception of the following: adequately treated basal cell or squamous cell carcinoma of the skin, carcinoma in situ of the cervix, or stable prostate cancer not requiring treatment | 2 | [
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NCT02544880 | 86:96:cancer,103:106:chronic_disease,110:127:treatment | Immunosuppression or immunocompromised for reasons not directly related to patient's malignancy (e.g. HIV or kidney transplant) | 2 | [
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NCT01964261 | 12:19:chronic_disease | History of seizure | 2 | [
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NCT03108950 | 16:22:chronic_disease | Diagnosed with stroke | 2 | [
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NCT03128008 | 39:73:cancer | Histologic/cytologic documentation of non-small cell lung cancer (NSCLC) | 2 | [
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NCT01807897 | 18:42:treatment,18:49:treatment,112:138:treatment,143:170:treatment | Current use of a positive airway pressure device (including continuous or bi-level positive airway pressure or adaptive servo-ventilation) or supplemental oxygen therapy | 2 | [
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NCT02473250 | 26:36:treatment,41:51:treatment,92:108:treatment,,143:152:treatment, | Previous failed trial of fluoxetine and citalopram by themselves or in combination with an anti-manic agent, defined as at least six weeks of treatment at the dose of 20 mg per day or more | 2 | [
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NCT01811368 | 1:23:chronic_disease | Hepatic encephalopathy | 2 | [
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NCT02058095 | 40:55:treatment | Current or anticipated future need for nitrate therapy | 2 | [
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NCT02914171 | 26:37:treatment | Individuals with current IV inotrope requirements | 2 | [
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NCT02577406 | 1:7:chronic_disease | stroke | 2 | [
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NCT01115283 | 37:46:chronic_disease | any ocular pathological conditions, nystagmus | 2 | [
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NCT02110069 | 1:26:chronic_disease,,,, | Kasabach Merritt Syndrome defined at a platelet counts less than 50,000 K/µl and/or fibrinogen level < 100 mg/dl at the time of diagnosis | 2 | [
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NCT03145181 | 25:41:cancer | Documented diagnosis of multiple myeloma according to International Myeloma Working Group (IMWG) diagnostic criteria | 2 | [
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NCT01220583 | 26:44:cancer | patients must be free of distant metastases based upon the following minimum diagnostic workup | 2 | [
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NCT02588326 | 13:21:chronic_disease,23:32:chronic_disease,34:55:chronic_disease,59:68:cancer,81:91:cancer | Presence of glaucoma, cataracts, ocular herpes simplex or carcinoma (other than basal cell) | 2 | [
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NCT02413970 | 34:37:chronic_disease | Likely suffer moderate-to-severe OSA based on history and physical | 2 | [
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NCT00716066 | 73:106:chronic_disease | Patients must satisfy the criteria for a diagnosis of one of the severe neurological autoimmune disorders outlined | 2 | [
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NCT02419560 | 29:32:cancer | Subject is at high risk for TLS | 2 | [
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NCT02495168 | 49:54:treatment, | patients should be able to withhold all inhaled SABAs for at least 6 hours prior to lung function assessments on study visits | 2 | [
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NCT02576444 | 1:18:chronic_disease,91:125:chronic_disease,144:161:treatment | Immunocompromised patients, e.g., patients who are known to be serologically positive for human immunodeficiency virus (HIV) and are receiving antiviral therapy (testing is not part of the protocol) | 2 | [
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NCT01942018 | 76:93:chronic_disease | Mechanical obstruction to esophageal outflow or infiltrative esophageal or gastric disorders | 2 | [
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NCT02188745 | 38:51:treatment,60:68:treatment,73:89:treatment,116:129:treatment,131:141:treatment,156:171:treatment,208:224:treatment | Combination regimens that include an anti-estrogen and any biologic, or targeted therapy, are permitted (e.g., any CDK inhibitor, everolimus, or any other novel biologics), and are considered to be a single hormonal therapy based regimen | 2 | [
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NCT02343549 | 41:53:allergy_name,90:94:allergy_name,98:106:allergy_name | History of hypersensitivity reaction to temozolomide or a history of hypersensitivity to DTIC or hydrogel | 2 | [
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NCT02468778 | 8:35:chronic_disease,68:85:treatment,130:152:treatment | Severe peripheral vascular disease that will preclude the use of a 14F access sheath, which is required for the insertion of the HeartMate PHP catheter | 2 | [
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NCT02542202 | 1:16:chronic_disease,20:36:chronic_disease,47:70:treatment | Acute bacterial or fungal infection requiring intravenous antibiotics at the time of registration | 2 | [
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NCT02885649 | 16:34:cancer | No evidence of metastatic disease on baseline imaging (chest x-ray [CXR] or chest CT, abdominal CT or MRI) | 2 | [
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NCT03036254 | 33:37:treatment | Subjects with an indication for HBOT | 2 | [
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NCT01185210 | 53:61:treatment,,,, | positive breath test after ingestion of 25 grams of fructose defined as either (a) ≥ 20 ppm rise of breath H2/CH4/both over baseline values or a successive rise of ≥ 5 ppm over baseline and in 3 consecutive breath samples | 2 | [
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NCT00065676 | 28:47:treatment,, | Subjects will be taken off hypoglycemic agents for 3 to 7 days prior to each part of the study | 2 | [
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NCT02947945 | 1:15:chronic_disease | Cardiomyopathy (established by echocardiography or MRI) | 2 | [
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NCT03008616 | 1:35:chronic_disease | antiphospholipid antibody syndrome | 2 | [
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NCT02393885 | 19:32:cancer,34:48:cancer,52:63:cancer | Has the following atrial myxoma, mural thrombus or mural tumor | 2 | [
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NCT01910818 | 8:22:chronic_disease,26:32:chronic_disease,,125:140:chronic_disease | Active Herpes Simplex or Zoster at the time of treatment or having experienced more than three episodes of Herpes Simplex / Zoster eruption within a year of study enrollment | 2 | [
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NCT02061293 | 14:24:treatment,69:86:treatment,94:109:treatment,111:125:treatment,127:143:treatment,145:155:treatment,178:190:treatment,194:213:treatment,215:222:treatment,224:239:treatment | Need to take medication with significant potential to interact with study medications (e.g., antidepressants, antipsychotics, psychostimulants, treatments for addictions, other dopaminergic or serotonergic agents, lithium, anticonvulsants) | 2 | [
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NCT02915744 | 1:14:treatment,36:47:treatment,39:47:treatment,66:84:treatment,94:107:treatment,111:117:treatment,123:135:treatment,137:156:treatment | prior therapy (administered in the neoadjuvant, adjuvant, and/or metastatic setting) with an anthracycline, a taxane, and capecitabine (prior anthracycline can be omitted if not medically appropriate or contraindicated for the patient) | 2 | [
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NCT01970176 | 40:55:treatment | Current or anticipated future need for nitrate therapy | 2 | [
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NCT02862938 | 5:24:treatment, | Any intraocular surgery of the study eye within 12 weeks prior to the screening visit | 2 | [
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NCT02990481 | 1:20:chronic_disease | unstable arrhythmia | 2 | [
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NCT01626079 | ,,70:74:treatment | a greater than 100% increase or greater than 50% decrease in dose of GDMT | 2 | [
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NCT03025139 | 20:27:treatment,29:38:treatment,47:70:treatment, | Have completed all surgery, radiation, and/or chemotherapy treatments at least 6 months previously | 2 | [
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NCT02574728 | 1:40:cancer | diffuse intrinsic pontine glioma (DIPG) | 2 | [
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NCT02236000 | 15:45:treatment,,96:114:treatment,137:153:treatment | Chronic daily treatment with corticosteroids with a dose of greater than or equal to 10 mg/day methylprednisolone equivalent (excluding inhaled steroids) | 2 | [
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NCT02881515 | 12:26:chronic_disease | history of kidney disease | 2 | [
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NCT02101736 | 35:44:chronic_disease | Patients who have an uncontrolled infection | 2 | [
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NCT02875301 | 1:9:chronic_disease | Dementia | 2 | [
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NCT01639508 | 8:28:chronic_disease | active peptic ulcer disease | 2 | [
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NCT03112824 | 1:7:treatment | SSRI's | 2 | [
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NCT02140255 | 1:19:chronic_disease, | Maternal infection must be confirmed, with confirmatory results available within 10 business days of enrollment | 2 | [
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NCT01841333 | ,,,44:57:chronic_disease | New York Heart Association Class III or IV heart failure | 2 | [
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NCT03054155 | 33:49:treatment | Patients unable to tolerate the laser treatments | 2 | [
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NCT01901562 | 25:34:allergy_name | Have a known allergy to lidocaine | 2 | [
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NCT02527421 | 55:66:allergy_name | Subjects who have a history of an adverse reaction to cosyntropin injection or similar test reagents | 2 | [
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NCT02579265 | 1:35:chronic_disease | spontaneous intestinal perforation | 2 | [
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NCT01871766 | 12:21:cancer,23:31:cancer,33:45:cancer,47:55:cancer,57:73:cancer,78:92:cancer,98:116:cancer | High-risk: Embryonal, botryoid, spindle cell, alveolar, undifferentiated, or anaplastic RMS with metastatic disease at diagnosis (stage 4) | 2 | [
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NCT02470897 | 1:16:chronic_disease,20:36:chronic_disease,47:70:treatment | Acute bacterial or fungal infection requiring intravenous antibiotics at the time of registration | 2 | [
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NCT02313428 | 1:9:chronic_disease | Diabetic | 2 | [
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NCT02393885 | 37:56:chronic_disease,92:103:chronic_disease,115:139:chronic_disease,143:157:chronic_disease | Uncorrected, reversible cause(s) of atrial fibrillation, or is currently being treated for arrhythmias other than atrial fibrillation (AF) or atrial flutter | 2 | [
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NCT02395614 | 26:69:treatment | candidates for immediate breast reconstruction with tissue expanders | 2 | [
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NCT02661386 | 1:14:treatment,29:36:treatment,40:46:treatment | Anticoagulant usage such as heparin or Plavix | 2 | [
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NCT02527200 | ,,,,182:189:chronic_disease | BMI (body mass index) corresponding to equal or above 30 kg/m^2 for adults by international cut-off points1 and equal or above the 95th percentile for age and sex (for diagnosis of obesity) | 2 | [
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NCT02724540 | ,44:62:treatment,64:68:treatment,70:78:treatment,82:89:treatment,119:148:treatment | Patients must be at least one month beyond prior chemotherapy, PRRT, ablation or surgery, and have recovered from all therapy-associated toxicities | 2 | [
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NCT02828592 | 10:22:chronic_disease | markedly hypocellular | 2 | [
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NCT02457845 | ,,96:111:treatment,127:137:cancer,153:173:treatment, | >24 Gy) or total body irradiation ≥ 3 months prior to study entry. Patients must have received focal radiation to symptomatic metastatic sites or local palliative radiation > 4 weeks prior to study entry | 2 | [
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