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NCT00099047 · FLOW

Participant flow

Celecoxib in Preventing Multiple Myeloma in Patients With Monoclonal Gammopathy or Smoldering Myeloma · Source last updated 2016-12-30

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

groups
  1. description
    Patients receive celecoxib PO BID for 6 months in the absence of unacceptable toxicity or progression to malignancy.
    id
    FG000
    title
    Arm I (Celecoxib)
  2. description
    Patients receive placebo PO BID for 6 months in the absence of unacceptable toxicity or progression to malignancy.
    id
    FG001
    title
    Arm II (Placebo)
periods
  1. milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        11
      2. group Id
        FG001
        num Subjects
        12
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        11
      2. group Id
        FG001
        num Subjects
        12
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        0
      2. group Id
        FG001
        num Subjects
        0
      type
      NOT COMPLETED
    title
    Overall Study
pre Assignment Details
There were no significant events or approaches utilized following enrollment but prior to group assignment.
recruitment Details
23 asymptomatic adult patients with a serum monoclonal protein \>1g/dL from Cleveland Clinic, Mayo Clinic, or University of Arkansas Medical Center were randomized between August 2005 and April 2008
Complete source fields
groups
  1. description
    Patients receive celecoxib PO BID for 6 months in the absence of unacceptable toxicity or progression to malignancy.
    id
    FG000
    title
    Arm I (Celecoxib)
  2. description
    Patients receive placebo PO BID for 6 months in the absence of unacceptable toxicity or progression to malignancy.
    id
    FG001
    title
    Arm II (Placebo)
periods
  1. milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        11
      2. group Id
        FG001
        num Subjects
        12
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        11
      2. group Id
        FG001
        num Subjects
        12
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        0
      2. group Id
        FG001
        num Subjects
        0
      type
      NOT COMPLETED
    title
    Overall Study
pre Assignment Details
There were no significant events or approaches utilized following enrollment but prior to group assignment.
recruitment Details
23 asymptomatic adult patients with a serum monoclonal protein \>1g/dL from Cleveland Clinic, Mayo Clinic, or University of Arkansas Medical Center were randomized between August 2005 and April 2008

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

Preserved source evidence · Not medical advice