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NCT00112489 · FLOW

Participant flow

Paclitaxel and Carboplatin in Treating Patients With Persistent or Recurrent Stage III or Stage IV Uterine Cancer · Source last updated 2018-09-25

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

groups
  1. description
    Paclitaxel 175 mg/m2 IV over 3 hours followed by Carboplatin AUC = 6 IV over 30 minutes repeated every 21 days until disease progression or adverse effects prohibit further therapy
    id
    FG000
    title
    Paclitaxel Followed by Carboplatin
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        8
      type
      Refused further treatment
    2. reasons
      1. group Id
        FG000
        num Subjects
        12
      type
      Adverse Event
    3. reasons
      1. group Id
        FG000
        num Subjects
        2
      type
      Death
    4. reasons
      1. group Id
        FG000
        num Subjects
        9
      type
      Other, Not Specified
    5. reasons
      1. group Id
        FG000
        num Subjects
        2
      type
      Patient never treated
    6. reasons
      1. group Id
        FG000
        num Subjects
        7
      type
      Ineligible
    milestones
    1. achievements
      1. comment
        All patients enrolled on study
        group Id
        FG000
        num Subjects
        55
      type
      STARTED
    2. achievements
      1. comment
        Completed regimen due to progression
        group Id
        FG000
        num Subjects
        15
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        40
      type
      NOT COMPLETED
    title
    Overall Study
Complete source fields
groups
  1. description
    Paclitaxel 175 mg/m2 IV over 3 hours followed by Carboplatin AUC = 6 IV over 30 minutes repeated every 21 days until disease progression or adverse effects prohibit further therapy
    id
    FG000
    title
    Paclitaxel Followed by Carboplatin
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        8
      type
      Refused further treatment
    2. reasons
      1. group Id
        FG000
        num Subjects
        12
      type
      Adverse Event
    3. reasons
      1. group Id
        FG000
        num Subjects
        2
      type
      Death
    4. reasons
      1. group Id
        FG000
        num Subjects
        9
      type
      Other, Not Specified
    5. reasons
      1. group Id
        FG000
        num Subjects
        2
      type
      Patient never treated
    6. reasons
      1. group Id
        FG000
        num Subjects
        7
      type
      Ineligible
    milestones
    1. achievements
      1. comment
        All patients enrolled on study
        group Id
        FG000
        num Subjects
        55
      type
      STARTED
    2. achievements
      1. comment
        Completed regimen due to progression
        group Id
        FG000
        num Subjects
        15
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        40
      type
      NOT COMPLETED
    title
    Overall Study

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

Preserved source evidence · Not medical advice