Study of characteristics and complications in young patients with myeloproliferative neoplasia
Official title: Children, Adolescents and Young Adults with Myeloproliferative Neoplasia: Study of Clinico-biological Characteristics and Complications
Run by University Hospital, Brest · NCT06715267 · Data updated 2026-11-12
This study is trying to gather information about young people under 30 with myeloproliferative neoplasia to better understand their health and complications.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 0 Years to 30 Years |
| Sex | All |
| Enrollment | 200 (estimated) |
| Sponsor | University Hospital, Brest Academic / other |
| Locations | 1 site (Brest) |
| Status | Recruiting |
| Started | April 1, 2023 |
| Main results expected | April 1, 2038 |
| Study ends | April 1, 2038 |
| Registry record updated | December 4, 2024 |
| Trial ID | NCT06715267 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are patients diagnosed with non-LMC myeloproliferative neoplasia before the age of 30.
✕Probably not a fit
Patients who refuse to participate or are under legal protection 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 observational study aims to create a national database that captures the clinico-biological characteristics and complications of myeloproliferative neoplasia in patients under 30 years old. By collecting and analyzing data from these patients, the study seeks to provide a clearer understanding of their care and outcomes. Additionally, it will facilitate the identification of biological samples available in routine laboratories, allowing researchers to conduct further analyses to refine diagnoses and explore new molecular prognostic factors.
Why it matters
Potential benefit: If successful, this study could enhance the understanding and management of myeloproliferative neoplasia in young patients, leading to improved treatment strategies.
How similar studies have gone: While this approach is focused on a specific age group and condition, similar observational studies have shown success in improving understanding of rare diseases.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patient diagnosed with non-LMC MPN before the age of 30 (PV or TE or MFP or PreMF) according to the 2016 WHO criteria. * Signature of the consent form for participation in the FIMBANK project. * Agreement to participate in the VYP study. * Patient of legal age at the time of inclusion in VYP. * Patient affiliated to a social security scheme Exclusion Criteria: * Refusal to participate by patients of full age * Patient under legal protection (guardianship, curatorship, etc.)
Where it's running
-
CHU de Brest
Brest, France Recruiting
Study contacts
- Study coordinator: Jean-Christophe IANOTTO
- Email: jean-christophe.ianotto@chu-brest.fr
- Phone: 0298223786
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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.