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NCT00803062 · FLOW

Participant flow

Paclitaxel and Cisplatin or Topotecan With or Without Bevacizumab in Treating Patients With Stage IVB, Recurrent, or Persistent Cervical Cancer · Source last updated 2019-07-23

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

groups
  1. description
    Paclitaxel 135 mg/m2 IV over 24 hrs on day 1 Cisplatin 50 mg/m2 IV on day 2 OR Paclitaxel 175 mg/m2 IV over 3 hrs on day 1 Cisplatin 50 mg/m2 IV on day 2 OR Paclitaxel 175 mg/m2 IV over 3 hrs on day 1 Cisplatin 50 mg/m2 IV on day 1 Cycles repeated q21 days to progression/toxicity
    id
    FG000
    title
    Arm I (Paclitaxel and Cisplatin)
  2. description
    Paclitaxel 135 mg/m2 IV over 24 hrs on day 1 Cisplatin 50 mg/m2 IV on day 2 Bevacizumab 15 mg/kg IV day 2 OR Paclitaxel 175 mg/m2 IV over 3 hrs on day 1 Cisplatin 50 mg/m2 IV on day 2 Bevacizumab 15 mg/kg IV day 2 OR Paclitaxel 175 mg/m2 IV over 3 hrs on day 1 Cisplatin 50 mg/m2 IV on day 1 Bevacizumab 15 mg/kg IV day 1 Cycles repeated q21 days to progression/toxicity
    id
    FG001
    title
    Arm II (Paclitaxel, Cisplatin, Bevacizumab)
  3. description
    Paclitaxel 175 mg/m2 over 3 hrs on day 1 Topotecan 0.75 mg/m2 over 30 mins days 1-3 Cycles repeated q21 days to progression/toxicity
    id
    FG002
    title
    Arm III (Topotecan Hydrochloride and Paclitaxel)
  4. description
    Paclitaxel 175 mg/m2 over 3 hrs on day 1 Topotecan 0.75 mg/m2 over 30 mins days 1-3 Bevacizumab 15 mg/kg IV day 1 Cycles repeated q21 days to progression/toxicity
    id
    FG003
    title
    Arm IV (Topotecan Hydrochloride, Paclitaxel, Bevacizumab)
periods
  1. milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        114
      2. group Id
        FG001
        num Subjects
        115
      3. group Id
        FG002
        num Subjects
        111
      4. group Id
        FG003
        num Subjects
        112
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        114
      2. group Id
        FG001
        num Subjects
        115
      3. group Id
        FG002
        num Subjects
        111
      4. group Id
        FG003
        num Subjects
        112
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        0
      2. group Id
        FG001
        num Subjects
        0
      3. group Id
        FG002
        num Subjects
        0
      4. group Id
        FG003
        num Subjects
        0
      type
      NOT COMPLETED
    title
    Overall Study
recruitment Details
The study was activated on 4/6/2009 and closed to accrual on 1/3/2012.
Complete source fields
groups
  1. description
    Paclitaxel 135 mg/m2 IV over 24 hrs on day 1 Cisplatin 50 mg/m2 IV on day 2 OR Paclitaxel 175 mg/m2 IV over 3 hrs on day 1 Cisplatin 50 mg/m2 IV on day 2 OR Paclitaxel 175 mg/m2 IV over 3 hrs on day 1 Cisplatin 50 mg/m2 IV on day 1 Cycles repeated q21 days to progression/toxicity
    id
    FG000
    title
    Arm I (Paclitaxel and Cisplatin)
  2. description
    Paclitaxel 135 mg/m2 IV over 24 hrs on day 1 Cisplatin 50 mg/m2 IV on day 2 Bevacizumab 15 mg/kg IV day 2 OR Paclitaxel 175 mg/m2 IV over 3 hrs on day 1 Cisplatin 50 mg/m2 IV on day 2 Bevacizumab 15 mg/kg IV day 2 OR Paclitaxel 175 mg/m2 IV over 3 hrs on day 1 Cisplatin 50 mg/m2 IV on day 1 Bevacizumab 15 mg/kg IV day 1 Cycles repeated q21 days to progression/toxicity
    id
    FG001
    title
    Arm II (Paclitaxel, Cisplatin, Bevacizumab)
  3. description
    Paclitaxel 175 mg/m2 over 3 hrs on day 1 Topotecan 0.75 mg/m2 over 30 mins days 1-3 Cycles repeated q21 days to progression/toxicity
    id
    FG002
    title
    Arm III (Topotecan Hydrochloride and Paclitaxel)
  4. description
    Paclitaxel 175 mg/m2 over 3 hrs on day 1 Topotecan 0.75 mg/m2 over 30 mins days 1-3 Bevacizumab 15 mg/kg IV day 1 Cycles repeated q21 days to progression/toxicity
    id
    FG003
    title
    Arm IV (Topotecan Hydrochloride, Paclitaxel, Bevacizumab)
periods
  1. milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        114
      2. group Id
        FG001
        num Subjects
        115
      3. group Id
        FG002
        num Subjects
        111
      4. group Id
        FG003
        num Subjects
        112
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        114
      2. group Id
        FG001
        num Subjects
        115
      3. group Id
        FG002
        num Subjects
        111
      4. group Id
        FG003
        num Subjects
        112
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        0
      2. group Id
        FG001
        num Subjects
        0
      3. group Id
        FG002
        num Subjects
        0
      4. group Id
        FG003
        num Subjects
        0
      type
      NOT COMPLETED
    title
    Overall Study
recruitment Details
The study was activated on 4/6/2009 and closed to accrual on 1/3/2012.

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Preserved source evidence · Not medical advice