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Trial · NCT01802333

Participant flow21

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDArm I (Standard Dose Cytarabine, Daunorubicin Hydrochloride)263
Overall StudySTARTEDArm II (High-dose Cytarabine, Idarubicin)267
Overall StudySTARTEDArm III (Vorinostat, High-dose Cytarabine, Idarubicin)224
Overall StudyHigh Risk PatientsArm I (Standard Dose Cytarabine, Daunorubicin Hydrochloride)60
Overall StudyHigh Risk PatientsArm II (High-dose Cytarabine, Idarubicin)61
Overall StudyHigh Risk PatientsArm III (Vorinostat, High-dose Cytarabine, Idarubicin)38
Overall StudyHigh Risk Patients Achieved CR/CRiArm I (Standard Dose Cytarabine, Daunorubicin Hydrochloride)38
Overall StudyHigh Risk Patients Achieved CR/CRiArm II (High-dose Cytarabine, Idarubicin)40
Overall StudyHigh Risk Patients Achieved CR/CRiArm III (Vorinostat, High-dose Cytarabine, Idarubicin)29
Overall StudyKnown NPM1 Status at BaselineArm I (Standard Dose Cytarabine, Daunorubicin Hydrochloride)169
Overall StudyKnown NPM1 Status at BaselineArm II (High-dose Cytarabine, Idarubicin)156
Overall StudyKnown NPM1 Status at BaselineArm III (Vorinostat, High-dose Cytarabine, Idarubicin)142
Overall StudyKnown Cytogenetic Risk at BaselineArm I (Standard Dose Cytarabine, Daunorubicin Hydrochloride)252
Overall StudyKnown Cytogenetic Risk at BaselineArm II (High-dose Cytarabine, Idarubicin)250
Overall StudyKnown Cytogenetic Risk at BaselineArm III (Vorinostat, High-dose Cytarabine, Idarubicin)210
Overall StudyCOMPLETEDArm I (Standard Dose Cytarabine, Daunorubicin Hydrochloride)214
Overall StudyCOMPLETEDArm II (High-dose Cytarabine, Idarubicin)206
Overall StudyCOMPLETEDArm III (Vorinostat, High-dose Cytarabine, Idarubicin)161
Overall StudyNOT COMPLETEDArm I (Standard Dose Cytarabine, Daunorubicin Hydrochloride)49
Overall StudyNOT COMPLETEDArm II (High-dose Cytarabine, Idarubicin)61

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this list from software.

Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT01802333/flow