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NCT00639769 · FLOW

Participant flow

Irinotecan and Cisplatin in Treating Patients With Recurrent or Metastatic Head and Neck Cancer · Source last updated 2012-09-14

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

groups
  1. description
    Cisplatin, Starting dose 30 mg/m2 Dose level -1 20 mg/m2; Irinotecan, Starting Dose 50 mg/m2, Dose level -1 40 mg/m2
    id
    FG000
    title
    Therapeutic Intervention
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        2
      type
      Death
    2. reasons
      1. group Id
        FG000
        num Subjects
        7
      type
      Adverse Event
    3. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Lack of Efficacy
    4. reasons
      1. group Id
        FG000
        num Subjects
        26
      type
      Disease progression
    5. reasons
      1. group Id
        FG000
        num Subjects
        4
      type
      Withdrawal by Subject
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        40
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        0
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        40
      type
      NOT COMPLETED
    title
    Overall Study
pre Assignment Details
A total of 41 people signed consent to take part in this study, of those, 1 was determined to be ineligible.
recruitment Details
Recruitment period = 2/27/2002 through 5/9/2006
Complete source fields
groups
  1. description
    Cisplatin, Starting dose 30 mg/m2 Dose level -1 20 mg/m2; Irinotecan, Starting Dose 50 mg/m2, Dose level -1 40 mg/m2
    id
    FG000
    title
    Therapeutic Intervention
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        2
      type
      Death
    2. reasons
      1. group Id
        FG000
        num Subjects
        7
      type
      Adverse Event
    3. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Lack of Efficacy
    4. reasons
      1. group Id
        FG000
        num Subjects
        26
      type
      Disease progression
    5. reasons
      1. group Id
        FG000
        num Subjects
        4
      type
      Withdrawal by Subject
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        40
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        0
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        40
      type
      NOT COMPLETED
    title
    Overall Study
pre Assignment Details
A total of 41 people signed consent to take part in this study, of those, 1 was determined to be ineligible.
recruitment Details
Recruitment period = 2/27/2002 through 5/9/2006

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Preserved source evidence · Not medical advice