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NCT03951220 · FLOW

Participant flow

The Development and Pilot Testing of a New MR Imaging Protocol to Quantify Myeloma Disease Burden and Bone Loss · Source last updated 2025-08-19

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

groups
  1. description
    Group 1a: New Myeloma; Group 1b: Relapsed Myeloma Group;1c: Smouldering Myeloma Baseline AND Follow-Up Assessment: Novel MR Whole body DXA scan Blood and urine samples QOL \& scan experience questionnaires
    id
    FG000
    title
    Group 1- Myeloma
  2. description
    Baseline AND Follow-Up Assessment: Novel MR Whole body DXA scan Blood and urine samples QOL \& scan experience questionnaires
    id
    FG001
    title
    Group 2- MGUS
  3. description
    Baseline Assessment ONLY: * Novel MR * QOL \& scan experience questionnaires
    id
    FG002
    title
    Group 3- Healthy Volunteers
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        9
      2. group Id
        FG001
        num Subjects
        2
      3. group Id
        FG002
        num Subjects
        0
      type
      Withdrawal by Subject
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        41
      2. group Id
        FG001
        num Subjects
        14
      3. group Id
        FG002
        num Subjects
        12
      comment
      Enrolment
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        41
      2. group Id
        FG001
        num Subjects
        14
      3. group Id
        FG002
        num Subjects
        12
      comment
      GROUP 1 \& 2 ASSESSMENT * Experimental MR * Whole body DXA scan * Blood and urine samples * QOL \& scan experience questionnaires GROUP 3 ASSESSMENT * Experimental MR * QOL \& scan experience questionnaires
      type
      Baseline Assessment
    3. achievements
      1. group Id
        FG000
        num Subjects
        32
      2. group Id
        FG001
        num Subjects
        12
      3. comment
        Group 3 participants did not attend follow-up
        group Id
        FG002
        num Subjects
        0
      comment
      GROUP 1 \& 2 ASSESSMENT * Experimental MR * Whole body DXA scan * Blood and urine samples * QOL \& scan experience questionnaires GROUP 3 ASSESSMENT • (No follow-up)
      type
      Follow-Up Assessment
    4. achievements
      1. group Id
        FG000
        num Subjects
        32
      2. group Id
        FG001
        num Subjects
        12
      3. group Id
        FG002
        num Subjects
        12
      type
      COMPLETED
    5. achievements
      1. group Id
        FG000
        num Subjects
        9
      2. group Id
        FG001
        num Subjects
        2
      3. group Id
        FG002
        num Subjects
        0
      type
      NOT COMPLETED
    title
    Overall Study
recruitment Details
Participants from Groups 1 and 2 were identified and approached by a healthcare professional in the oncology clinic at the Churchill Hospital, Oxford. Group 3 participants were typically partners of the participants from Groups 1 and 2 and were recruited at the same time.
Complete source fields
groups
  1. description
    Group 1a: New Myeloma; Group 1b: Relapsed Myeloma Group;1c: Smouldering Myeloma Baseline AND Follow-Up Assessment: Novel MR Whole body DXA scan Blood and urine samples QOL \& scan experience questionnaires
    id
    FG000
    title
    Group 1- Myeloma
  2. description
    Baseline AND Follow-Up Assessment: Novel MR Whole body DXA scan Blood and urine samples QOL \& scan experience questionnaires
    id
    FG001
    title
    Group 2- MGUS
  3. description
    Baseline Assessment ONLY: * Novel MR * QOL \& scan experience questionnaires
    id
    FG002
    title
    Group 3- Healthy Volunteers
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        9
      2. group Id
        FG001
        num Subjects
        2
      3. group Id
        FG002
        num Subjects
        0
      type
      Withdrawal by Subject
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        41
      2. group Id
        FG001
        num Subjects
        14
      3. group Id
        FG002
        num Subjects
        12
      comment
      Enrolment
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        41
      2. group Id
        FG001
        num Subjects
        14
      3. group Id
        FG002
        num Subjects
        12
      comment
      GROUP 1 \& 2 ASSESSMENT * Experimental MR * Whole body DXA scan * Blood and urine samples * QOL \& scan experience questionnaires GROUP 3 ASSESSMENT * Experimental MR * QOL \& scan experience questionnaires
      type
      Baseline Assessment
    3. achievements
      1. group Id
        FG000
        num Subjects
        32
      2. group Id
        FG001
        num Subjects
        12
      3. comment
        Group 3 participants did not attend follow-up
        group Id
        FG002
        num Subjects
        0
      comment
      GROUP 1 \& 2 ASSESSMENT * Experimental MR * Whole body DXA scan * Blood and urine samples * QOL \& scan experience questionnaires GROUP 3 ASSESSMENT • (No follow-up)
      type
      Follow-Up Assessment
    4. achievements
      1. group Id
        FG000
        num Subjects
        32
      2. group Id
        FG001
        num Subjects
        12
      3. group Id
        FG002
        num Subjects
        12
      type
      COMPLETED
    5. achievements
      1. group Id
        FG000
        num Subjects
        9
      2. group Id
        FG001
        num Subjects
        2
      3. group Id
        FG002
        num Subjects
        0
      type
      NOT COMPLETED
    title
    Overall Study
recruitment Details
Participants from Groups 1 and 2 were identified and approached by a healthcare professional in the oncology clinic at the Churchill Hospital, Oxford. Group 3 participants were typically partners of the participants from Groups 1 and 2 and were recruited at the same time.

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Preserved source evidence · Not medical advice