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NCT00564889 · FLOW

Participant flow

Lenalidomide, Cyclophosphamide, and Dexamethasone in Treating Patients With Primary Systemic Amyloidosis · Source last updated 2013-05-14

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

groups
  1. description
    Lenalidomide (Len) 15mg daily (days 1-21) Cyclophosphamide (Cyc) 300 mg/m\^2 (days 1, 8, 15) Dexamethasone (Dex) 40 mg weekly
    id
    FG000
    title
    Len/Cyc/Dex
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        7
      type
      Death
    2. reasons
      1. group Id
        FG000
        num Subjects
        12
      type
      Adverse Event
    3. reasons
      1. group Id
        FG000
        num Subjects
        3
      type
      Alternative treatment
    4. reasons
      1. group Id
        FG000
        num Subjects
        3
      type
      Disease progression
    5. reasons
      1. group Id
        FG000
        num Subjects
        4
      type
      Other, not specified
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        35
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        6
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        29
      type
      NOT COMPLETED
    title
    Overall Study
recruitment Details
Thirty-five(35) participants were recruited between December 2007 and November 2008 at Mayo Clinic.
Complete source fields
groups
  1. description
    Lenalidomide (Len) 15mg daily (days 1-21) Cyclophosphamide (Cyc) 300 mg/m\^2 (days 1, 8, 15) Dexamethasone (Dex) 40 mg weekly
    id
    FG000
    title
    Len/Cyc/Dex
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        7
      type
      Death
    2. reasons
      1. group Id
        FG000
        num Subjects
        12
      type
      Adverse Event
    3. reasons
      1. group Id
        FG000
        num Subjects
        3
      type
      Alternative treatment
    4. reasons
      1. group Id
        FG000
        num Subjects
        3
      type
      Disease progression
    5. reasons
      1. group Id
        FG000
        num Subjects
        4
      type
      Other, not specified
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        35
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        6
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        29
      type
      NOT COMPLETED
    title
    Overall Study
recruitment Details
Thirty-five(35) participants were recruited between December 2007 and November 2008 at Mayo Clinic.

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Preserved source evidence · Not medical advice