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NCT00503997 · FLOW

Participant flow

Pemetrexed and Oxaliplatin in Treating Patients With Locally Advanced Head and Neck Cancer · Source last updated 2012-05-10

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

groups
  1. description
    Patients receive pemetrexed disodium IV and oxaliplatin IV over 2 hours on day 1. Treatment repeats every 14 days for up to 4 courses. If patient progresses before receiving 4 courses of treatment, treatment will be discontinued and patient will proceed to surgery.
    id
    FG000
    title
    Pemetrexed/Oxaliplatin
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      disease progression
    2. reasons
      1. group Id
        FG000
        num Subjects
        5
      type
      Adverse Event
    3. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Death
    4. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Withdrawal by Subject
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        42
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        34
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        8
      type
      NOT COMPLETED
    title
    Overall Study
pre Assignment Details
This study consented 42 patients. One patient was found ineligible.
recruitment Details
The trial was open to accrual from 12/13/2006 to 4/9/2008.
Complete source fields
groups
  1. description
    Patients receive pemetrexed disodium IV and oxaliplatin IV over 2 hours on day 1. Treatment repeats every 14 days for up to 4 courses. If patient progresses before receiving 4 courses of treatment, treatment will be discontinued and patient will proceed to surgery.
    id
    FG000
    title
    Pemetrexed/Oxaliplatin
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      disease progression
    2. reasons
      1. group Id
        FG000
        num Subjects
        5
      type
      Adverse Event
    3. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Death
    4. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Withdrawal by Subject
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        42
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        34
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        8
      type
      NOT COMPLETED
    title
    Overall Study
pre Assignment Details
This study consented 42 patients. One patient was found ineligible.
recruitment Details
The trial was open to accrual from 12/13/2006 to 4/9/2008.

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Preserved source evidence · Not medical advice