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NCT00819832 · FLOW

Participant flow

Anderson Circulating Tumor Cell Burden (CTCB) Study · Source last updated 2023-03-24

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

groups
  1. description
    Vertebroplasty
    id
    FG000
    title
    Phase 1 Group 1 Vertebroplasty
  2. description
    Kyphoplasty
    id
    FG001
    title
    Phase 1 Group 2 Kyphoplasty
  3. description
    Vertebroplasty
    id
    FG002
    title
    Phase 2 Group 1 Vertebroplasty
  4. description
    Vertebroplasty with Cavity SpineWand
    id
    FG003
    title
    Phase 2 Group 2 Vertebroplasty +Cavity SpineWand
  5. description
    Kyphoplasty
    id
    FG004
    title
    Phase 2 Group 3 Kyphoplasty
  6. description
    Kyphoplasty with Cavity SpineWand
    id
    FG005
    title
    Phase 2 Group 4 Kyphoplasty + Cavity SpineWand
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        3
      2. group Id
        FG001
        num Subjects
        0
      3. group Id
        FG002
        num Subjects
        0
      4. group Id
        FG003
        num Subjects
        0
      5. group Id
        FG004
        num Subjects
        0
      6. group Id
        FG005
        num Subjects
        0
      type
      Sponsor Termination of Study
    milestones
    1. achievements
      1. comment
        No patient data analysis.
        group Id
        FG000
        num Subjects
        3
      2. group Id
        FG001
        num Subjects
        0
      3. group Id
        FG002
        num Subjects
        0
      4. group Id
        FG003
        num Subjects
        0
      5. group Id
        FG004
        num Subjects
        0
      6. group Id
        FG005
        num Subjects
        0
      type
      STARTED
    2. 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
      5. group Id
        FG004
        num Subjects
        0
      6. group Id
        FG005
        num Subjects
        0
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        3
      2. group Id
        FG001
        num Subjects
        0
      3. group Id
        FG002
        num Subjects
        0
      4. group Id
        FG003
        num Subjects
        0
      5. group Id
        FG004
        num Subjects
        0
      6. group Id
        FG005
        num Subjects
        0
      type
      NOT COMPLETED
    title
    Overall Study
pre Assignment Details
Study terminated by sponsor. No patient data analysis performed due to the limited amount of data gathered from the study's three participants.
recruitment Details
Recruitment Period: December 30, 2008 to March 29, 2010. All recruitment done at UT MD Anderson Cancer Center.
Complete source fields
groups
  1. description
    Vertebroplasty
    id
    FG000
    title
    Phase 1 Group 1 Vertebroplasty
  2. description
    Kyphoplasty
    id
    FG001
    title
    Phase 1 Group 2 Kyphoplasty
  3. description
    Vertebroplasty
    id
    FG002
    title
    Phase 2 Group 1 Vertebroplasty
  4. description
    Vertebroplasty with Cavity SpineWand
    id
    FG003
    title
    Phase 2 Group 2 Vertebroplasty +Cavity SpineWand
  5. description
    Kyphoplasty
    id
    FG004
    title
    Phase 2 Group 3 Kyphoplasty
  6. description
    Kyphoplasty with Cavity SpineWand
    id
    FG005
    title
    Phase 2 Group 4 Kyphoplasty + Cavity SpineWand
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        3
      2. group Id
        FG001
        num Subjects
        0
      3. group Id
        FG002
        num Subjects
        0
      4. group Id
        FG003
        num Subjects
        0
      5. group Id
        FG004
        num Subjects
        0
      6. group Id
        FG005
        num Subjects
        0
      type
      Sponsor Termination of Study
    milestones
    1. achievements
      1. comment
        No patient data analysis.
        group Id
        FG000
        num Subjects
        3
      2. group Id
        FG001
        num Subjects
        0
      3. group Id
        FG002
        num Subjects
        0
      4. group Id
        FG003
        num Subjects
        0
      5. group Id
        FG004
        num Subjects
        0
      6. group Id
        FG005
        num Subjects
        0
      type
      STARTED
    2. 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
      5. group Id
        FG004
        num Subjects
        0
      6. group Id
        FG005
        num Subjects
        0
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        3
      2. group Id
        FG001
        num Subjects
        0
      3. group Id
        FG002
        num Subjects
        0
      4. group Id
        FG003
        num Subjects
        0
      5. group Id
        FG004
        num Subjects
        0
      6. group Id
        FG005
        num Subjects
        0
      type
      NOT COMPLETED
    title
    Overall Study
pre Assignment Details
Study terminated by sponsor. No patient data analysis performed due to the limited amount of data gathered from the study's three participants.
recruitment Details
Recruitment Period: December 30, 2008 to March 29, 2010. All recruitment done at UT MD Anderson Cancer Center.

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Preserved source evidence · Not medical advice