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NCT00335140 · FLOW

Participant flow

Rituximab and Combination Chemotherapy in Treating Patients With Primary Central Nervous System Lymphoma · Source last updated 2023-07-03

Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.

groups
  1. description
    rituximab cytarabine dexamethasone leucovorin calcium methotrexate procarbazine hydrochloride vincristine sulfate
    id
    FG000
    title
    Rituximab + Standard Chemotherapy
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Ineligible
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        26
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        25
      type
      Eligible
    3. achievements
      1. group Id
        FG000
        num Subjects
        25
      type
      Treated
    4. achievements
      1. group Id
        FG000
        num Subjects
        25
      type
      COMPLETED
    5. achievements
      1. group Id
        FG000
        num Subjects
        1
      type
      NOT COMPLETED
    title
    Overall Study
recruitment Details
Participants were recruited from ECOG-ACRIN member institutions starting 12/21/2006 and accrued its first patient on 08/23/2007. The study was suspended 2/24/2010 for interim analysis. After the interim analysis, it was determined that the goals of the study had been met and the study was closed on 4/12/2013.
Complete source fields
groups
  1. description
    rituximab cytarabine dexamethasone leucovorin calcium methotrexate procarbazine hydrochloride vincristine sulfate
    id
    FG000
    title
    Rituximab + Standard Chemotherapy
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Ineligible
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        26
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        25
      type
      Eligible
    3. achievements
      1. group Id
        FG000
        num Subjects
        25
      type
      Treated
    4. achievements
      1. group Id
        FG000
        num Subjects
        25
      type
      COMPLETED
    5. achievements
      1. group Id
        FG000
        num Subjects
        1
      type
      NOT COMPLETED
    title
    Overall Study
recruitment Details
Participants were recruited from ECOG-ACRIN member institutions starting 12/21/2006 and accrued its first patient on 08/23/2007. The study was suspended 2/24/2010 for interim analysis. After the interim analysis, it was determined that the goals of the study had been met and the study was closed on 4/12/2013.

Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f

Preserved source evidence · Not medical advice