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NCT02070549 | 1:18:cancer | Colorectal cancer patients | {
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NCT01901562 | 15:27:treatment, | Have received chemotherapy in the last 12 months | {
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NCT02535312 | 16:22:treatment,118:136:treatment,,,,,,,425:436:treatment | The effects of TRC102 on the developing human fetus are unknown; for this reason and because TRC102 as well as other therapeutic agents used in this trial are known to be teratogenic, women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry, for the duration of study participation, and 4 months after completion of the study drugs | {
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NCT02516670 | 16:38:chronic_disease | Has history of calcium oxalate stones | {
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NCT02061553 | 12:34:chronic_disease,43:56:chronic_disease,58:83:chronic_disease,104:120:chronic_disease | History of serious mental illness such as schizophrenia, schizo-affective disorder, or well-documented bipolar disorder | {
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NCT02620579 | 1:24:chronic_disease | neurological impairment of the in the upper-extremity (determined by loss of sensation, muscle weakness, and reflex changes) | {
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NCT01524536 | ,18:28:treatment | Receiving >10 mg prednisone or equivalent at the time of enrollment | {
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NCT03028012 | 1:13:chronic_disease | Fibromyalgia | {
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NCT00488696 | 21:36:chronic_disease | Serious systemic or groin infection | {
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NCT02046395 | 1:16:chronic_disease | Type 2 Diabetes | {
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NCT02389959 | 17:46:treatment,54:75:treatment,77:95:chronic_disease | actively taking immunosuppressive medications due to organ transplantation, rheumatoid disease, or other medical conditions | {
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NCT01415882 | ,,,,201:211:treatment | Pregnant women or women of reproductive ability who are unwilling to use 2 effective methods of contraception from the time of signing the informed consent form through 90 days after the last dose of study drug | {
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NCT02008136 | 8:14:chronic_disease | recent stroke | {
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NCT02453373 | 1:24:chronic_disease | Ventricular tachycardia | {
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NCT02008136 | 8:27:chronic_disease,29:37:chronic_disease,41:49:chronic_disease | Severe psychiatric illness, dementia or delirium | {
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NCT02485639 | 14:37:chronic_disease | a history of Guillain-Barre syndrome | {
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NCT01742338 | 36:43:chronic_disease,45:61:chronic_disease,65:70:chronic_disease | Alternative diagnosis for cause of dyspnea, increased sputum or cough | {
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NCT01895777 | 1:18:chronic_disease | Renal dysfunction | {
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NCT02663908 | 1:25:cancer | Advanced prostate cancer | {
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NCT01175044 | 15:40:chronic_disease,50:53:chronic_disease,54:58:chronic_disease | Patients with chronic immunosuppression (such as HIV/AIDS) | {
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NCT01891318 | 18:27:treatment,70:85:treatment,90:99:treatment | Patient can have prior SRS to lesions other than the one planned for neoadjuvant SRS and resection | {
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NCT02530034 | 29:47:cancer | Patients must have relapsed/refractory disease | {
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NCT02428205 | 55:66:treatment,68:76:chronic_disease,78:111:chronic_disease,113:128:chronic_disease,130:146:chronic_disease,160:167:chronic_disease,169:190:chronic_disease,235:248:allergy_name,, | Any of the following exclusionary criteria related to propranolol (diabetes, reactive airway/pulmonary disease, thyroid disease, bradyarrhythmias, unexplained syncope, narrow angle glaucoma, known hypersensitivity/adverse reaction to beta-blockers, potentially interacting drugs, underweight < 15 kg) | {
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NCT01653093 | 19:26:chronic_disease | Patients who have cardiac | {
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NCT02111850 | 38:60:treatment | Patients who are receiving any other investigational agents | {
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NCT01415752 | ,,,45:58:chronic_disease,60:79:chronic_disease,101:124:chronic_disease,129:149:treatment,168:176:chronic_disease | Patients must not have NYHA Class III or IV heart failure, uncontrolled angina, severe uncontrolled ventricular arrhythmias, or electrocardiographic evidence of acute ischemia | {
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NCT02132130 | 33:47:chronic_disease,49:62:chronic_disease,64:93:chronic_disease,128:144:treatment,148:165:treatment | Any otological history, such as chronic otitis, cholesteatoma, tympanic membrane perforation, that suggests poor candidacy for cochlear implant or inner ear surgery or suggests potential interference with study auditory or vestibular function tests | {
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NCT02873598 | 21:32:allergy_name | Contraindication to IV contrast | {
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NCT02460900 | 20:28:chronic_disease,, | Meets criteria for dementia by scoring below 10 on the Hopkins HIV Dementia Scale | {
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NCT03066648 | 11:14:chronic_disease | High risk MDS | {
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NCT02429934 | 30:53:treatment | Inability to self-administer subcutaneous injections, to comply with instructions, or to keep appointments for study visits | {
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NCT03059888 | 26:38:treatment, | Subject has received any live vaccine within 3 months of screening | {
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NCT02826681 | 8:41:chronic_disease | Active acute or known chronic infections | {
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NCT02471430 | 65:83:allergy_name,84:102:allergy_name,106:118:allergy_name | History of anaphylaxis, allergy or serious adverse reactions to Interferon-alpha2a/Interferon-alpha2b or panobinostat | {
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NCT03034213 | 23:46:chronic_disease | Suspected presence of enterocutaneous fistula | {
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NCT02356848 | 1:22:treatment | Prior foot amputation | {
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NCT01815359 | 46:56:cancer | Presence of clinically apparent or suspected metastasis to sites other than lymph nodes or peritoneal surfaces | {
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NCT00959140 | 13:34:chronic_disease | evidence of progressive infection by imaging studies | {
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NCT02418195 | 1:12:chronic_disease | polymyalgia | {
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NCT01920061 | 15:19:cancer,44:64:treatment,72:82:cancer | Patients with TNBC with no prior cytotoxic chemotherapy therapy in the metastatic setting | {
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NCT03179163 | ,42:69:treatment | Women are post-menopausal and not taking hormone replacement therapy | {
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NCT01743950 | 25:49:treatment | May not be on full dose anti-coagulation therapy | {
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NCT01261728 | 1:27:treatment | prior intravesical therapy | {
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NCT01992861 | 31:34:treatment,, | for the test-retest sub-study MRI, patients must have a GFR of > 60 mL/min/1.73m^2 | {
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NCT02440815 | 1:15:treatment,23:36:treatment,,64:89:treatment, | Antidepressant use or psychotherapy within the past 6 weeks or electroconvulsive therapy within the past 6 months | {
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NCT01620216 | 105:117:treatment | certain agents that prolong the corrected QT interval may be allowed but only after discussion with the chemotherapy pharmacist | {
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NCT03062462 | ,,,104:120:treatment, | PAgR is more than 46% and the percentage of inhibition of ADP-induced platelet aggregation measured by thrombelastogram is not more than 30% | {
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NCT02583893 | 13:37:chronic_disease | symptomatic congestive heart failure | {
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NCT02321501 | 30:59:chronic_disease,61:74:chronic_disease,83:92:chronic_disease,94:121:chronic_disease,127:144:chronic_disease,164:181:chronic_disease,164:175:chronic_disease,263:280:chronic_disease | active (acute or chronic) or uncontrolled severe infection, liver disease such as cirrhosis, decompensated liver disease, and chronic hepatitis (i.e. quantifiable hepatitis B virus test [HBV-DNA] and/or positive hepatitis B surface antigen [HbsAg], quantifiable hepatitis C virus test [HCV-RNA]) | {
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NCT02266329 | ,398:413:treatment | Participation in a headache support group or other activity such as meditation or yoga intended to mitigate headache or other chronic pain must be stable for at least 4 weeks prior to beginning the preliminary screening period and should be intended to be continued for the duration of the trial. Participants will be encouraged to defer enrolling in such activities until they have completed the treatment trial | {
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NCT01988246 | ,,71:87:treatment | Central subfield macular thickness ≤ 320 μm in the study eye prior to cataract surgery as determined by SD-OCT and confirmed by the reading center | {
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NCT02653287 | 110:113:chronic_disease | include meeting at least 4 of 11 American College of Rheumatology (ACR) classification criteria for definite SLE, or 3 out of 11 ACR classification criteria with also meeting at least one SLICC criteria | {
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NCT02376153 | 1:18:treatment | Acetabular repair with instrumentation | {
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NCT02349867 | 13:31:cancer | Evidence of metastatic disease | {
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NCT02253316 | 13:15:cancer | Evidence of MM disease progression any time prior to enrollment | {
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NCT01241708 | 14:23:chronic_disease,25:30:chronic_disease,32:38:chronic_disease,42:62:chronic_disease | Uncontrolled bacterial, viral, fungal or parasitic infections | {
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NCT01810588 | 1:29:chronic_disease | Chronic lymphocytic leukemia, relapsed or with poor prognostic features | {
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NCT02466009 | 25:35:cancer, | History of other active malignancy within past 2 years | {
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NCT02159703 | 1:37:chronic_disease | symptomatic congestive heart failure | {
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NCT02513797 | 29:42:chronic_disease | Documented history of right heart failure specifically when right ventricle exceeds the left ventricular size | {
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NCT01996449 | 17:40:chronic_disease,42:70:chronic_disease,74:94:chronic_disease,98:114:treatment | Any evidence of cardiopulmonary disease, left ventricular hypertrophy or systolic dysfunction by echocardiography | {
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NCT02730481 | 43:54:cancer | Histologically or cytologically confirmed solid tumor that is metastatic or unresectable and for which standard curative or palliative measures do not exist or are no longer effective | {
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NCT03101085 | 16:22:cancer,39:51:treatment,55:72:treatment, | any history of cancer that required a chemotherapy or radiation therapy intervention within the past 5 years | {
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NCT01364467 | 10:29:chronic_disease | signs of bacterial infection | {
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NCT02361554 | 28:46:chronic_disease | Subject has a diagnosis of mental retardation | {
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NCT02377089 | 1:16:chronic_disease, | suicide attempt within six months | {
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NCT01835626 | 1:17:treatment | Prior vismodegib or other antagonists of the Hh pathway | {
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NCT02278198 | 18:37:treatment,57:71:cancer,86:104:cancer,145:187:treatment | status post near total thyroidectomy for differentiated thyroid cancer without known distant metastases and who are planning to undergo routine remnant thyroid tissue ablation with I-131 | {
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NCT02004028 | 11:31:treatment,, | Use of an investigational drug within 28 days or 5 half-lives prior to first dose | {
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NCT01175044 | 31:63:treatment | Patients scheduled to undergo revision total knee arthroplasty for infectious reasons | {
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NCT00919503 | 382:399:treatment | DONOR: HLA-matched sibling cord blood exclusions: Any cord blood units that have not passed donor screening for infectious disease markers as recommended by the National Marrow Donor Project (NMDP) will not be used unless a waiver is signed by the clinical attending allowing use of cord blood unit; cord blood units are presumed to be cytomegalovirus (CMV) negative regardless of serologic testing due to passive transmission of maternal CMV antibodies | {
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NCT02584647 | 32:37:cancer,41:76:cancer,78:109:cancer, | Examples of the latter include basal or squamous cell carcinoma of the skin, in-situ carcinoma of the cervix, and isolated elevation of prostate-specific antigen | {
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NCT02421341 | 25:35:chronic_disease | No history of dangerous arrhythmia's | {
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NCT02078102 | 30:73:treatment, | Patients must not have taken nonsteroidal antiinflammatory drugs (NSAID) in the past 14 days before treatment on this protocol | {
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NCT02540330 | 27:56:cancer,60:84:cancer,95:105:treatment | Pathological diagnosis of Invasive Ductal Breast Cancer or Ductal Carcinoma in Situ requiring mastectomy | {
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NCT03127358 | 20:33:treatment | Willing to receive HCV treatment on-site at DoSA clinics | {
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NCT02192359 | 31:37:treatment,47:55:treatment,57:68:treatment,70:79:treatment,84:96:treatment,,131:146:treatment | Use of drugs known to inhibit UGT1A1, such as atazanir, gemfibrozil, indinavir, or ketoconazole, within 2 weeks prior to start of study treatment | {
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NCT03152409 | 14:31:chronic_disease | History of a bleeding disorder | {
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NCT02725177 | 14:25:chronic_disease | Patient with sarcoidosis | {
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"chronic_disease": "sarcoidosis",
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0,
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NCT02538198 | 15:36:chronic_disease, | Patients with myocardial infarction within 6 months prior to enrollment | {
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NCT02124772 | 1:12:cancer | Solid tumor cohort (B1) specific criteria | {
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NCT01572480 | 62:89:cancer | Patients must have histologically or cytologically confirmed Smoldering Multiple Myeloma confirmed by the Laboratory of Pathology, NCI or the Department of Laboratory Medicine, CC based on the International Myeloma Working Group Criteria | {
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NCT01072370 | 19:38:chronic_disease | Presence of known chromosomal anomaly | {
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NCT01760655 | ,16:41:chronic_disease | Greater than 3 cytogenetic abnormalities or any one of the following cytogenetic abnormalities | {
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NCT00969332 | 20:33:chronic_disease | Documented case of liver disease other than Parenteral Nutrition Associated Cholestasis | {
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NCT03007745 | 1:22:chronic_disease | myocardial infarction | {
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} | [
0,
0
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"myocardial",
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NCT02561104 | 14:30:treatment | Referred for cataract surgery at Parkland Memorial Hospital | {
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"treatment": "cataract surgery"
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NCT02419495 | 28:43:cancer,37:43:cancer,,97:102:cancer,106:141:cancer | Diagnosis or recurrence of invasive cancer other than the present cancer within 3 years (except basal or squamous cell carcinoma of the skin that has been definitively treated) | {
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NCT02400255 | 1:23:chronic_disease | Uncontrolled infection | {
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} | [
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"Uncontrolled",
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NCT02905370 | 23:39:treatment | Referred to home care physical therapy following acute medical deconditioning | {
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NCT02567227 | 5:22:chronic_disease,26:44:treatment,56:68:treatment,133:149:chronic_disease,, | Any medical condition or chronic medication use (e.g., neuroleptics) that will compromise safety or affect cognitive functioning or terminal illness with life expectancy less than 12 months | {
"allergy_name": null,
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NCT01962415 | 1:4:chronic_disease | HIV negative | {
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"chronic_disease": "HIV",
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} | [
2,
0
] | [
"HIV",
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] | 185 |
NCT01942018 | 1:33:treatment | Prior esophageal Botox injection | {
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"treatment": "Prior esophageal Botox injection"
} | [
0,
3,
1,
1
] | [
"Prior",
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] | 3,940 |
NCT02047474 | 21:39:treatment | No other concurrent anticancer therapy | {
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"treatment": "anticancer therapy"
} | [
0,
0,
0,
0,
1
] | [
"No",
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] | 1,054 |
NCT01945814 | 23:26:treatment,28:35:treatment,46:92:treatment, | Patients who received ATG, Campath, or other T cell immunosuppressive monoclonal antibodies in the last 28 days | {
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"treatment": "T cell immunosuppressive monoclonal antibodies"
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NCT02513797 | 16:34:treatment,67:86:treatment,91:104:cancer | Any history of thoracic radiation with the exception of localized radiation treatment for breast cancer | {
"allergy_name": null,
"cancer": "breast cancer",
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NCT03028350 | 8:12:treatment,16:33:treatment,40:50:treatment,, | Use of oral or systemic steroids (e.g. prednisone or equivalent) > 20 mg daily in the last four weeks before starting treatment | {
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NCT01742182 | 14:27:chronic_disease | Diagnosis of idiopathic PD as defined by the United Kingdom PD Society Brain Bank Criteria | {
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"chronic_disease": "idiopathic PD",
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NCT02324387 | 1:18:chronic_disease | nodal involvement (N0 - N3) | {
"allergy_name": null,
"cancer": null,
"chronic_disease": "nodal involvement",
"treatment": null
} | [
2,
0,
0,
0,
0
] | [
"nodal",
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] | 4,601 |
NCT02863991 | ,,,,70:74:treatment | Platelets ≥75,000/mm3 without platelet transfusion ≤ 3 days prior to C1D1 | {
"allergy_name": null,
"cancer": null,
"chronic_disease": null,
"treatment": "C1D1"
} | [
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] | 2,796 |
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