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NCT02427841 | ,,,,156:168:treatment,,, | Women of child-bearing potential and men must be willing to use adequate contraception during the entire study and for 8 weeks following completion of all chemotherapy on study; this includes hormonal or barrier method, or abstinence | 1 | [
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NCT02416206 | ,43:55:treatment | Within 9 months of the start of induction chemotherapy and no evidence of relapse or progression | 1 | [
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NCT02359825 | 12:24:treatment | undergoing chemotherapy | 1 | [
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NCT02320292 | 19:31:treatment | No indication for chemotherapy | 1 | [
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NCT02315196 | ,81:93:treatment | imaging must have been performed no greater than 30 days prior to initiation of chemotherapy | 1 | [
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NCT02309892 | 10:22:treatment | Previous chemotherapy | 1 | [
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NCT02308709 | 12:24:treatment | Concurrent chemotherapy is allowed, but not required | 1 | [
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NCT02303977 | ,41:53:treatment | Pregnant or breast-feeding patients, as chemotherapy is thought to present substantial risk to the fetus/infant | 1 | [
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NCT02227199 | 54:66:treatment | Patients must be anticipated to complete 2 cycles of chemotherapy | 1 | [
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NCT02203513 | ,147:159:treatment | Patients should have recurrent platinum-resistant, defined as disease recurrence by imaging within 6 months of the last receipt of platinum-based chemotherapy | 1 | [
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NCT02159703 | 7:19:treatment, | Prior chemotherapy within the past 5 years | 1 | [
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NCT02153229 | ,62:74:treatment | Subjects who have received more than 2 doses of neo-adjuvant chemotherapy | 1 | [
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NCT02135588 | ,40:52:treatment | At least 2 days from administration of chemotherapy | 1 | [
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NCT02128906 | ,,53:65:treatment | Pregnant women are excluded from this study because chemotherapy | 1 | [
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NCT02128906 | 24:36:treatment | breast feeding because chemotherapy | 1 | [
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NCT02115295 | 74:86:treatment | Patient with documented hypersensitivity to any of the components of the chemotherapy program | 1 | [
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NCT02101736 | 21:33:treatment, | No myelosuppressive chemotherapy within 4 weeks of study entry | 1 | [
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NCT02099591 | 49:61:treatment | Patients currently receiving the first cycle of chemotherapy | 1 | [
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NCT02091999 | 1:13:treatment | chemotherapy | 1 | [
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NCT02037048 | ,40:52:treatment | for 90 days following the last dose of chemotherapy | 1 | [
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NCT02031250 | 43:55:treatment | Patients must be able to receive protocol chemotherapy in the judgment of the treating Medical Oncologist | 1 | [
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NCT01953900 | 53:65:treatment | Recovered from the acute toxic effects of all prior chemotherapy | 1 | [
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NCT01928589 | 73:85:treatment | Patient must have a Medical Oncology consult with the recommendation of chemotherapy | 1 | [
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NCT01925573 | 58:70:treatment | 6 weeks since the completion of a nitrosourea-containing chemotherapy regimen | 1 | [
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NCT01919619 | ,,,,128:140:treatment, | diffusing capacity of the lung for carbon monoxide (DLCO) >= 40% within 3 months of study entry (or within 1 month if received chemotherapy within the past 3 months) | 1 | [
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NCT01901562 | 15:27:treatment, | Have received chemotherapy in the last 12 months | 1 | [
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NCT01896999 | 46:58:treatment | Patients must have relapsed after first line chemotherapy | 1 | [
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NCT01871766 | ,189:201:treatment | Participants treated on this protocol in the low or intermediate risk arm who experience disease progression prior to week 13 will transfer to the high risk arm and proceed with high risk chemotherapy starting at week 1 of the protocol | 1 | [
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NCT01859819 | 13:25:treatment | No previous chemotherapy | 1 | [
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NCT01807091 | ,,,87:99:treatment | Treatment-related mortality (TRM) score < 9.21 corresponding to a TRM rate of 3% when chemotherapy of similar intensity as proposed here is administered to inpatients | 1 | [
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NCT01754298 | 1:13:treatment | chemotherapy treatment | 1 | [
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NCT01730794 | 37:49:treatment | Immunosuppressed patients receiving chemotherapy | 1 | [
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NCT01703949 | ,63:75:treatment | Patients must be anticipated to complete at least 2 cycles of chemotherapy on study | 1 | [
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NCT01690468 | 31:43:treatment | At least one prior regimen of chemotherapy, with no maximum number of chemotherapy cycles | 1 | [
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NCT01676259 | 1:13:treatment | chemotherapy | 1 | [
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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 | 1 | [
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NCT01614990 | 38:50:treatment | subjects may otherwise be undergoing chemotherapy | 1 | [
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NCT01526603 | 43:55:treatment, | Patients who are delayed in consolidation chemotherapy beyond 8 weeks | 1 | [
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NCT01526603 | 40:52:treatment | Recovery from last induction course of chemotherapy | 1 | [
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NCT01515527 | 74:86:treatment | Patient with documented hypersensitivity to any of the components of the chemotherapy program | 1 | [
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NCT01505569 | 48:60:treatment | Timing: Recovery from last induction course of chemotherapy | 1 | [
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NCT01434316 | 7:19:treatment | Prior chemotherapy | 1 | [
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NCT01238120 | 63:75:treatment | Patients with a neutropenic episode during the first cycle of chemotherapy or at high risk for a neutropenic episode during future chemotherapy cycles at the treating physicians discretion | 1 | [
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NCT01061515 | 41:53:treatment | All patients must be consented prior to chemotherapy | 1 | [
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NCT01061515 | 53:65:treatment,,,, | Patients must have adequate renal function prior to chemotherapy defined as serum creatinine ≤ 2.0 mg/dl or creatinine clearance ≥60 ml.min/1.73 m² for patients with creatinine levels above 2.0 mg/dl | 1 | [
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NCT01061515 | 105:117:treatment | must undergo a peritoneal scan documenting at least one working intraperitoneal port prior to receiving chemotherapy | 1 | [
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NCT00911560 | ,,178:190:treatment | stage 4 with (any age) or without (>18 months old) MYCN amplification, MYCN-amplified stage 3 (unresectable; any age), MYCN-amplified stage 4S, or disease resistant to standard chemotherapy | 1 | [
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NCT00719888 | ,,97:109:treatment | ligible with (M2 marrow) with =< 25% blasts in marrow after having failed one or more cycles of chemotherapy | 1 | [
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NCT00896493 | 14:38:chronic_disease,42:48:chronic_disease | Uncontrolled congestive heart failure or angina | 1 | [
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NCT03060473 | 8:32:chronic_disease,, | Active congestive heart failure (EF<45%) | 1 | [
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NCT03030859 | 1:25:chronic_disease | congestive heart failure | 1 | [
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NCT03028012 | 14:38:chronic_disease | Pre-existing congestive heart failure | 1 | [
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NCT03008408 | 23:47:chronic_disease,,, | History of documented congestive heart failure (New York Heart Association functional classification III-IV) | 1 | [
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NCT02986815 | 23:47:chronic_disease | NYHA class III and IV congestive heart failure | 1 | [
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NCT02931110 | ,,,41:65:chronic_disease | New York Heart Association Class 3 or 4 congestive heart failure | 1 | [
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NCT02807272 | 49:73:chronic_disease | New York Heart Association grade III or greater congestive heart failure | 1 | [
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NCT02755116 | 54:78:chronic_disease | New York Heart Association (NYHA) Class II or higher congestive heart failure | 1 | [
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NCT02596776 | 1:25:chronic_disease | congestive heart failure | 1 | [
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NCT02576301 | 13:37:chronic_disease | Symptomatic congestive heart failure | 1 | [
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NCT02567422 | 13:37:chronic_disease, | Symptomatic congestive heart failure (requiring hospital stay within the last 6 months) | 1 | [
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NCT02525861 | 44:68:chronic_disease,,, | The participant has clinically significant congestive heart failure with New York Heart Association (NYHA) Class III/IV symptoms | 1 | [
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NCT02489045 | 28:52:chronic_disease, | Patients with uncontrolled congestive heart failure (NYHA Class IV) | 1 | [
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NCT02446236 | 29:53:chronic_disease | Uncontrolled or symptomatic congestive heart failure | 1 | [
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NCT02442635 | ,,53:77:chronic_disease | Have New York Heart Association class II or greater congestive heart failure | 1 | [
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NCT02411773 | 22:46:chronic_disease,, | Clinical evidence of congestive heart failure or ejection fraction below 35% | 1 | [
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NCT02353728 | 1:25:chronic_disease | congestive heart failure | 1 | [
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NCT02343549 | ,55:79:chronic_disease | New York Heart Association (NYHA) Grade II or greater congestive heart failure | 1 | [
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NCT02321501 | 23:47:chronic_disease,,, | history of documented congestive heart failure (New York Heart Association functional classification III-IV) | 1 | [
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NCT02314377 | ,,71:95:chronic_disease | Patients must not have New York Heart Association Grade II or greater congestive heart failure | 1 | [
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NCT02272998 | 26:50:chronic_disease | Patients with history of congestive heart failure are excluded | 1 | [
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NCT02257424 | ,20:44:chronic_disease, | Current ≥ Class II congestive heart failure as defined by New York Heart Association | 1 | [
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NCT02253316 | ,,,33:57:chronic_disease | uncompensated NYHA Class 3 or 4 congestive heart failure | 1 | [
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