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NCT00410826 · FLOW

Participant flow

Cisplatin and Radiation Therapy With or Without Erlotinib Hydrochloride in Treating Patients With Stage III or Stage IV Head and Neck Cancer · Source last updated 2013-05-10

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

groups
  1. description
    Patients receive cisplatin IV on days 1, 22, and 43 and undergo 3-dimensional conformal or intensity modulated radiotherapy once daily, 5 days per week, on days 1-47.
    id
    FG000
    title
    Arm A (Cisplatin and Radiotherapy)
  2. description
    Patients receive cisplatin and radiotherapy as in Arm A. Patients also receive erlotinib hydrochloride PO QD on days -7 to 47.
    id
    FG001
    title
    Arm B (Cisplatin, Radiotherapy, Erlotinib)
periods
  1. milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        105
      2. group Id
        FG001
        num Subjects
        99
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        96
      2. group Id
        FG001
        num Subjects
        95
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        9
      2. group Id
        FG001
        num Subjects
        4
      type
      NOT COMPLETED
    title
    Overall Study
recruitment Details
Patients were randomized between December 2006 and October 2011.
Complete source fields
groups
  1. description
    Patients receive cisplatin IV on days 1, 22, and 43 and undergo 3-dimensional conformal or intensity modulated radiotherapy once daily, 5 days per week, on days 1-47.
    id
    FG000
    title
    Arm A (Cisplatin and Radiotherapy)
  2. description
    Patients receive cisplatin and radiotherapy as in Arm A. Patients also receive erlotinib hydrochloride PO QD on days -7 to 47.
    id
    FG001
    title
    Arm B (Cisplatin, Radiotherapy, Erlotinib)
periods
  1. milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        105
      2. group Id
        FG001
        num Subjects
        99
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        96
      2. group Id
        FG001
        num Subjects
        95
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        9
      2. group Id
        FG001
        num Subjects
        4
      type
      NOT COMPLETED
    title
    Overall Study
recruitment Details
Patients were randomized between December 2006 and October 2011.

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Preserved source evidence · Not medical advice