Clinical trial Recruiting at 1 site Observational Ages 18 and up

Study of proteins involved in red blood cell production

Official title: POlycythemia, Proteins and ErYthropoiesis

Run by Centre Hospitalier Universitaire Dijon · NCT06905106 · Data updated 2026-11-12

This study looks at the proteins that help make red blood cells to see how they work in people with polycythemia and related conditions.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment400 (estimated)
SponsorCentre Hospitalier Universitaire Dijon
Academic / other
Locations1 site (Dijon)
StatusRecruiting
StartedSeptember 1, 2024
Main results expectedSeptember 2028
Study endsSeptember 2028
Registry record updatedApril 1, 2025
Trial IDNCT06905106 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates include patients diagnosed with polycythemia or those with related conditions but without polycythemia.

Probably not a fit

Patients who are pregnant, minors, or unable to provide consent will 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 focuses on understanding the various proteins that regulate erythropoiesis, the process of red blood cell production. It aims to analyze blood samples from patients with polycythemia and those with related conditions to quantify and qualify the proteins involved in this regulation. Key proteins of interest include erythropoietin, interleukin-3, and those related to iron metabolism. The study will help elucidate the complex mechanisms that control erythrocyte production and the factors leading to excessive red blood cell production.

Why it matters

Potential benefit: If successful, this study could enhance our understanding of erythropoiesis and lead to better management of conditions like polycythemia.

How similar studies have gone: While the study explores established concepts in erythropoiesis, its specific focus on protein regulation in polycythemia is relatively novel.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

\- Persons who have given their non-opposition

Patients with polycythemia:

* haemoglobin value \> 16 g/dl female or \> 16.5 g/dl male
* with a well-identified cause: either primary (polycythemia Vaquez, erythropoietin receptor or LNK/SH2B3 mutation...) or secondary \[cardio-respiratory pathologies, renal pathologies (post-transplant, polycystic kidney disease), metabolic pathologies, tumour (leiomyoma, pheochromocytoma...), constitutional mutations (hyperaffine haemoglobins, HIF2/EPAS1, PHD/EGLN1, VHL, ...)

Patients control:

\- persons with a similar pathology to that of polycythemia patients, essentialy secondary, but without polycythemia, i.e. with a haemoglobin value of \< 16 g/DL for women and \< 16.5 g/DL for men

Exclusion Criteria:

* Person subject to a measure of legal protection (guardianship, tutorship)
* Person subject to a court order
* Pregnant, parturient or nursing woman
* Incapable of expressing consent
* Minor

Where it's running

  • CHU Dijon Bourgogne
    Dijon, 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.