Clinical trial Recruiting at 1 site Observational Ages 18 to 99

Using MRI to assess myelofibrosis

Official title: Quantitative MRI for Myelofibrosis - MRI Parameters as Biomarkers for Analyzing Extent of Disease and Measuring Response to Treatment

Run by University of Michigan Rogel Cancer Center · NCT01973881 · Data updated 2026-11-12

This study is testing if special MRI scans can help doctors see how severe myelofibrosis is and how well treatments are working for patients.

Quick facts

Study typeObservational
Ages18 Years to 99 Years
SexAll
Enrollment192 (estimated)
SponsorUniversity of Michigan Rogel Cancer Center
Academic / other
Locations1 site (Ann Arbor, Michigan)
StatusRecruiting
StartedDecember 22, 2014
Main results expectedDecember 2026
Study endsDecember 2026
Registry record updatedJuly 31, 2026
Trial IDNCT01973881 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include adults over 18 diagnosed with primary myelofibrosis or its post-polycythemia vera and post-essential thrombocythemia forms.

Probably not a fit

Patients with contraindications to MRI, such as those with pacemakers or other magnetic devices, may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study focuses on developing and validating functional MRI parameters as biomarkers to analyze the extent of myelofibrosis and quantify treatment responses. Researchers will utilize diffusion MRI and T1-weighted imaging to evaluate water and fat content in bone marrow, aiming to identify changes that predict therapy effectiveness. The goal is to establish MRI techniques that can provide earlier insights into disease severity and treatment response compared to current clinical measures. This foundational research may pave the way for larger trials assessing existing and new therapies for myelofibrosis.

Why it matters

Potential benefit: If successful, this study could enable earlier detection of treatment responses in myelofibrosis patients, leading to more timely and effective management of the disease.

How similar studies have gone: While this approach is innovative, similar studies using advanced MRI techniques have shown promise in other conditions, suggesting potential for success in this context.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Male /female subjects over the age of 18
2. Diagnosis of primary myelofibrosis, post-polycythemia vera myelofibrosis, or post-essential thrombocythemia myelofibrosis.
3. No contraindications to MRI
4. Able to undergo MRI without anesthesia

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Exclusion Criteria:

1. Patients with pacemakers or other implanted magnetic devices that may malfunction or move because of the strong magnetic field inside the MRI room and scanner.
2. Any prior adverse event associated with MRI that is not related to injection of contrast agents or other medicines.

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Where it's running

  • University of Michigan Hospital
    Ann Arbor, Michigan, United States
    Recruiting

Study contacts

  • Principal investigator: Gary Luker, M.D. — University of Michigan Hospital
  • Study coordinator: Gary Luker, M.D.
  • Email: gluker@umich.edu
  • Phone: 734-763-5476

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.