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NCT01348607 · FLOW

Participant flow

Methylphenidate HCl or Modafinil in Treating Young Patients With Excessive Daytime Sleepiness After Cancer Therapy · Source last updated 2014-02-21

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

groups
  1. description
    Patients receive oral methylphenidate extended-release once daily for 7-42 days in the absence of unacceptable toxicity.
    id
    FG000
    title
    Arm I - Methylphenidate Hydrochloride
  2. description
    Patients receive oral modafinil once daily for 7-42 days in the absence of unacceptable toxicity.
    id
    FG001
    title
    Arm II -Modafinil
  3. description
    Patients receive oral placebo once daily for 7-42 days in the absence of unacceptable toxicity.
    id
    FG002
    title
    Arm III Placebo
periods
  1. milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        1
      2. group Id
        FG001
        num Subjects
        0
      3. group Id
        FG002
        num Subjects
        0
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        1
      2. group Id
        FG001
        num Subjects
        0
      3. group Id
        FG002
        num Subjects
        0
      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
      type
      NOT COMPLETED
    title
    Overall Study
Complete source fields
groups
  1. description
    Patients receive oral methylphenidate extended-release once daily for 7-42 days in the absence of unacceptable toxicity.
    id
    FG000
    title
    Arm I - Methylphenidate Hydrochloride
  2. description
    Patients receive oral modafinil once daily for 7-42 days in the absence of unacceptable toxicity.
    id
    FG001
    title
    Arm II -Modafinil
  3. description
    Patients receive oral placebo once daily for 7-42 days in the absence of unacceptable toxicity.
    id
    FG002
    title
    Arm III Placebo
periods
  1. milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        1
      2. group Id
        FG001
        num Subjects
        0
      3. group Id
        FG002
        num Subjects
        0
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        1
      2. group Id
        FG001
        num Subjects
        0
      3. group Id
        FG002
        num Subjects
        0
      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
      type
      NOT COMPLETED
    title
    Overall Study

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Preserved source evidence · Not medical advice