Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Testing Optical Genome Mapping in Ph-Negative Myeloproliferative Neoplasms

Official title: Evaluation of Optical Genome Mapping in Phi Negative Myeloproliferative Neoplasia in the Detection of Acquired Cytogenetic Abnormalities

Run by Centre Hospitalier Universitaire, Amiens · NCT05714592 · Data updated 2026-11-12

This study tests whether Optical Genome Mapping can better detect chromosomal changes in adults with Ph-negative myeloproliferative neoplasms who need bone marrow cytogenetics.

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment300 (estimated)
SponsorCentre Hospitalier Universitaire, Amiens
Academic / other
Locations1 site (Amiens, Picardie)
StatusRecruiting
StartedMay 17, 2023
Main results expectedMay 18, 2027
Study endsMay 18, 2027
Registry record updatedMay 28, 2026
Trial IDNCT05714592 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults 18 years or older with polycythemia vera, essential thrombocythemia, or primary/secondary myelofibrosis who require bone marrow cytogenetics at diagnosis or follow-up and can understand French.

Probably not a fit

Patients whose disease biology or sample quality limits the usefulness of OGM may not receive additional benefit beyond standard methods.

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

What this trial studies

This interventional study evaluates Optical Genome Mapping (OGM) as a high-resolution method to identify structural and copy-number variations across the genome in Ph-negative myeloproliferative neoplasms. Eligible participants are adults with polycythemia vera, essential thrombocythemia, or myelofibrosis who require bone marrow cytogenetics. A peripheral blood or bone marrow sample will be analyzed using OGM to determine its sensitivity and potential to replace or supplement standard cytogenetic methods. The study aims to improve prognostic stratification by detecting abnormalities that may be missed by conventional techniques. Results will inform whether OGM can be integrated into routine cytogenetic characterization of hematologic malignancies.

Why it matters

Potential benefit: If successful, patients may receive more precise cytogenetic information that could improve prognosis and guide treatment decisions.

How similar studies have gone: Previous studies suggest optical genome mapping has potential to enhance cytogenetic characterization in hematologic disorders, but broader clinical validation is ongoing.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Patient 18 years of age or older
* Diagnosis or follow-up of polycythemia vera, essential thrombocythemia or primary or secondary myelofibrosis
* Requires bone marrow cytogenetics at diagnosis or follow-up
* Understanding of the French language
* Information of the patient and collection of no objection
* Person affiliated to a social security regime

Exclusion Criteria:

* Patient with BCR::ABL positive myeloproliferative neoplasia.
* Person with a medical history that may impair the ability to understand the information notice

Where it's running

  • Centre Hospitalier Universitaire d'Amiens
    Amiens, Picardie, France
    Recruiting

Study contacts

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.