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NCT01827384 | 89:98:treatment | patients on other trials will be eligible as long as they are no longer receiving study treatment | 1 | [
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NCT01827384 | ,,99:108:treatment | radiofrequency ablation (RFA) of localized lesions should have been performed >= 2 weeks prior to treatment | 1 | [
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NCT01822522 | ,68:77:treatment | Any of the following within 28 days before the first dose of study treatment | 1 | [
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NCT01822522 | ,,,100:109:treatment | Hemoptysis of >= 0.5 teaspoon (2.5 mL) of red blood within 3 months before the first dose of study treatment | 1 | [
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NCT01822522 | ,,,,,195:204:treatment | The participant has prothrombin time (PT)/international normalized ratio (INR) or partial thromboplastin time (PTT) test >= 1.3 x the laboratory ULN within 7 days before the first dose of study treatment | 1 | [
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NCT01817751 | ,,,117:126:treatment | Any other hemorrhage/bleeding event >= grade 3 (NCI CTCAE v4.0) within 4 weeks or less prior to first dose of study treatment | 1 | [
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NCT01817751 | ,,,121:130:treatment | Women of childbearing potential must have a negative serum pregnancy test performed within 7 days prior to the start of treatment | 1 | [
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NCT01811498 | ,,124:133:treatment | Patients must agree to use a medically effective method of contraception during and for a period of three months after the treatment period | 1 | [
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NCT01804634 | 58:67:treatment | Patients must be willing to participate in all stages of treatment | 1 | [
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NCT01794793 | ,,,131:140:treatment | In case of use of oral contraception women should have been stable on the same pill for a minimum of 3 months before taking study treatment | 1 | [
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NCT01794793 | 58:67:treatment | Willingness and ability to comply with scheduled visits, treatment plans and any other study procedures | 1 | [
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NCT01787409 | 61:70:treatment | During the Active Monitoring Phase of a study (i.e., active treatment and observation), participants must be willing to return to the consenting institution for follow-up | 1 | [
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NCT01776190 | 49:58:treatment, | You are unable to come in three days a week for treatment for a 10-week period | 1 | [
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NCT01763970 | ,,79:88:treatment | refusal of women of child bearing potential to take a pregnancy test prior to treatment | 1 | [
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NCT01742299 | 58:67:treatment | Willingness and ability to comply with scheduled visits, treatment plans and any other study procedures | 1 | [
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NCT01720836 | ,,59:68:treatment | Subjects must be within 4 to 12 weeks of standard of care treatment for their particular stage of disease | 1 | [
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NCT01720836 | ,63:72:treatment | Subjects must not be more than 12 weeks from standard of care treatment for their particular stage of disease | 1 | [
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NCT01670877 | ,,77:86:treatment, | Men must agree and commit to use a barrier method of contraception while on treatment and for 3 months after the last dose of the investigational product | 1 | [
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NCT01620216 | ,,175:184:treatment | Female and male patients who are fertile must agree to use an effective form of contraception with their sexual partners from randomization through 4 months after the end of treatment | 1 | [
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NCT01620216 | ,100:109:treatment | Persons of reproductive potential must agree to use an adequate method of contraception throughout treatment | 1 | [
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NCT01581749 | 58:67:treatment | implanted hardware or other material that would prohibit treatment planning or delivery | 1 | [
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NCT01562626 | ,,,82:91:treatment | women must have a negative serum or urine pregnancy test 1 week before beginning treatment on this trial | 1 | [
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NCT01532687 | 32:41:treatment | must be willing to comply with treatment and follow-up | 1 | [
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NCT01495637 | 20:29:treatment | Persistence (after treatment) of any of the following in the PICU before enrollment: | 1 | [
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NCT01367444 | 33:42:treatment | Enrolment in any other clinical treatment study throughout the duration of the SAR422459 study | 1 | [
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NCT01366612 | ,,,,90:99:treatment | unwilling to use acceptable birth control methods (men or women) for twelve months after treatment | 1 | [
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NCT01312857 | ,,54:63:treatment | Calcium ≥ lower limit of normal (≤ 48 hours prior to treatment start.) | 1 | [
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NCT01312857 | ,,31:40:treatment | Lab values ≤ 14 days prior to treatment start: | 1 | [
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NCT01312857 | ,,56:65:treatment | Magnesium ≥ lower limit of normal (≤ 48 hours prior to treatment start.) | 1 | [
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NCT01312857 | ,36:45:treatment | Renal function (≤ 14 days prior to treatment start) | 1 | [
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NCT01306045 | ,222:231:treatment | Individuals who meet the eligibility criteria for EGFR germline mutation testing but who do not have advanced cancer as defined in 3.1.1 may enroll for EGFR germline mutation testing only and will not be eligible for the treatment or NOS arms | 1 | [
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NCT01269853 | ,,124:133:treatment | Patients must agree to use a medically effective method of contraception during and for a period of three months after the treatment period | 1 | [
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NCT01261728 | 31:40:treatment | Supportive care trials or non-treatment trials, e.g. QOL | 1 | [
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NCT01220583 | ,,,123:132:treatment, | Women of childbearing potential and male participants who are sexually active must practice adequate contraception during treatment and for 6 weeks following treatment | 1 | [
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NCT01174121 | ,,136:145:treatment | Patients of both genders must be willing to practice birth control from the time of enrollment on this study and for four months after treatment | 1 | [
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NCT01174121 | 18:27:treatment | The experimental treatment being evaluated in this protocol depends on an intact immune system | 1 | [
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NCT00472329 | ,,,,99:108:treatment | Fertile men or women unwilling to use contraceptive techniques during and for 12 months following treatment | 1 | [
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NCT03099590 | 24:32:chronic_disease | laboratory evidence of diabetes | 1 | [
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NCT03041844 | 81:89:chronic_disease | DUs must be present on the ankle or foot and be secondary to complications from diabetes | 1 | [
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NCT02927639 | 19:27:chronic_disease, | Have been seen in diabetes clinic in the last 6 months | 1 | [
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NCT02857283 | 1:9:chronic_disease | diabetes requiring medication | 1 | [
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NCT02823665 | 59:67:chronic_disease | Healthy non-surgical patients with no personal history of diabetes | 1 | [
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NCT02823665 | 56:64:chronic_disease | Healthy non-surgical patients with personal history of diabetes | 1 | [
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NCT02798458 | 14:22:chronic_disease,, | Uncontrolled diabetes with a hemoglobin A1C greater than 10 | 1 | [
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NCT02772562 | 14:22:chronic_disease | Uncontrolled diabetes | 1 | [
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NCT02751866 | 1:9:chronic_disease | diabetes | 1 | [
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NCT02723266 | 23:31:chronic_disease | signs and symptoms of diabetes | 1 | [
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NCT02690116 | 14:22:chronic_disease | Uncontrolled diabetes (fatigue-related factor) | 1 | [
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NCT02682147 | 1:9:chronic_disease | diabetes | 1 | [
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NCT02578732 | 14:22:chronic_disease | Uncontrolled diabetes. If patient has diabetes, confirmation on status (controlled or uncontrolled) required at registration | 1 | [
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NCT02555280 | 14:22:chronic_disease | Uncontrolled diabetes | 1 | [
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NCT02531932 | 14:22:chronic_disease,, | uncontrolled diabetes as defined by fasting serum glucose >1.5 x ULN | 1 | [
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NCT02522494 | 14:22:chronic_disease | Drug-induced diabetes | 1 | [
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NCT02462161 | 13:21:chronic_disease | Preexisting diabetes | 1 | [
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NCT02430077 | 32:40:chronic_disease,,,, | Previous clinical diagnosis of diabetes mellitus or fasting blood glucose ≥ 126 mg/dL or hemoglobin A1c ≥ 6.5% | 1 | [
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NCT02417701 | 26:34:chronic_disease,, | Patients with controlled diabetes are allowed on study; controlled diabetes is defined as fetal bovine serum (FBS) =< 130 mg/dL in the context of this study | 1 | [
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NCT02408120 | 36:44:chronic_disease | Hyperglycemia without a history of diabetes | 1 | [
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NCT02373644 | 1:9:chronic_disease | diabetes | 1 | [
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NCT02347995 | 38:46:chronic_disease,,,, | untreated and / or poorly controlled diabetes with fasting blood glucose of greater than 170 and HbA1c greater than 10.0 | 1 | [
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NCT02329652 | 1:9:chronic_disease | diabetes or any condition which requires frequent blood pressure monitoring or frequent venipuncture | 1 | [
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NCT02253368 | 1:9:chronic_disease | diabetes | 1 | [
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NCT02245841 | 28:36:chronic_disease | Patients with uncontrolled diabetes | 1 | [
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NCT02244814 | 23:31:chronic_disease | suspected preexisting diabetes | 1 | [
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NCT02226159 | 1:9:chronic_disease,, | diabetes (type I or type II) | 1 | [
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NCT02219581 | 15:23:chronic_disease | Patients with diabetes | 1 | [
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NCT02169037 | 1:9:chronic_disease | diabetes (1 point) | 1 | [
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NCT02139436 | 1:9:chronic_disease | diabetes | 1 | [
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NCT02095808 | 19:27:chronic_disease | Poorly controlled diabetes | 1 | [
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NCT02087826 | 60:68:chronic_disease | Currently taking any medications used for the treatment of diabetes | 1 | [
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NCT01954966 | 1:9:chronic_disease | diabetes | 1 | [
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NCT01905046 | ,,74:82:chronic_disease | Patients with hemoglobin a1c > 6.3 or who are being actively treated for diabetes | 1 | [
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NCT01883258 | 12:20:chronic_disease | history of diabetes | 1 | [
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NCT01807897 | 19:27:chronic_disease,, | Poorly controlled diabetes (HbA1c > 9.0) | 1 | [
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NCT01803451 | 25:33:chronic_disease | healthy control without diabetes | 1 | [
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NCT01653080 | 12:20:chronic_disease | History of diabetes | 1 | [
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NCT01627301 | 1:9:chronic_disease | diabetes | 1 | [
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NCT01573429 | 14:22:chronic_disease | Uncontrolled diabetes | 1 | [
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NCT01422746 | 23:31:chronic_disease,,,, | Previous diagnosis of diabetes, fasting glucose ≥126 mg/dL, or a hemoglobin A1c ≥6.5% | 1 | [
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