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NCT00820248 · FLOW

Participant flow

Radiation + Cisplatin or Panitumumab in Locally Advanced Stage III or Stage IV Head and Neck Cancer · Source last updated 2023-08-22

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

groups
  1. description
    Patients undergo standard fractionation radiotherapy (IMRT or 3D CRT) once daily, 5 days a week, for 7 weeks. Patients receive cisplatin IV over 1 hour on days 1, 22, and 43 of radiotherapy. cisplatin: Given IV 3-dimensional conformal radiation therapy: Patients undergo radiotherapy intensity-modulated radiation therapy: Patients undergo radiotherapy
    id
    FG000
    title
    Cisplatin
  2. description
    Patients undergo accelerated fractionation radiotherapy (IMRT or 3D CRT) once or twice daily, 5 days a week, for 6 weeks. Patients receive panitumumab IV over 30-90 minutes 1 week prior to and on days 15 and 36 of radiotherapy. panitumumab: Given IV 3-dimensional conformal radiation therapy: Patients undergo radiotherapy accelerated radiation therapy: Patients undergo accelerated fractionation radiotherapy intensity-modulated radiation therapy: Patients undergo radiotherapy
    id
    FG001
    title
    Panitumumab
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        4
      2. group Id
        FG001
        num Subjects
        1
      type
      No treated
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        160
      2. group Id
        FG001
        num Subjects
        160
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        156
      2. group Id
        FG001
        num Subjects
        159
      comment
      Only treated patients were evaluated for adverse event.
      type
      Received Protocol Treatment
    3. achievements
      1. group Id
        FG000
        num Subjects
        156
      2. group Id
        FG001
        num Subjects
        159
      type
      COMPLETED
    4. achievements
      1. group Id
        FG000
        num Subjects
        4
      2. group Id
        FG001
        num Subjects
        1
      type
      NOT COMPLETED
    title
    Overall Study
Complete source fields
groups
  1. description
    Patients undergo standard fractionation radiotherapy (IMRT or 3D CRT) once daily, 5 days a week, for 7 weeks. Patients receive cisplatin IV over 1 hour on days 1, 22, and 43 of radiotherapy. cisplatin: Given IV 3-dimensional conformal radiation therapy: Patients undergo radiotherapy intensity-modulated radiation therapy: Patients undergo radiotherapy
    id
    FG000
    title
    Cisplatin
  2. description
    Patients undergo accelerated fractionation radiotherapy (IMRT or 3D CRT) once or twice daily, 5 days a week, for 6 weeks. Patients receive panitumumab IV over 30-90 minutes 1 week prior to and on days 15 and 36 of radiotherapy. panitumumab: Given IV 3-dimensional conformal radiation therapy: Patients undergo radiotherapy accelerated radiation therapy: Patients undergo accelerated fractionation radiotherapy intensity-modulated radiation therapy: Patients undergo radiotherapy
    id
    FG001
    title
    Panitumumab
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        4
      2. group Id
        FG001
        num Subjects
        1
      type
      No treated
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        160
      2. group Id
        FG001
        num Subjects
        160
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        156
      2. group Id
        FG001
        num Subjects
        159
      comment
      Only treated patients were evaluated for adverse event.
      type
      Received Protocol Treatment
    3. achievements
      1. group Id
        FG000
        num Subjects
        156
      2. group Id
        FG001
        num Subjects
        159
      type
      COMPLETED
    4. achievements
      1. group Id
        FG000
        num Subjects
        4
      2. group Id
        FG001
        num Subjects
        1
      type
      NOT COMPLETED
    title
    Overall Study

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

Preserved source evidence · Not medical advice