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 type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 300 (estimated) |
| Sponsor | Centre Hospitalier Universitaire, Amiens Academic / other |
| Locations | 1 site (Amiens, Picardie) |
| Status | Recruiting |
| Started | May 17, 2023 |
| Main results expected | May 18, 2027 |
| Study ends | May 18, 2027 |
| Registry record updated | May 28, 2026 |
| Trial ID | NCT05714592 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
- Study coordinator: Valentin Lestringant, MD
- Email: Lestringant.valentin@chu-amiens.fr
- Phone: 03 22 08 70 23
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.