Actively Recruiting
Blood Viscosity in Polycythemia Patients
Led by Hospices Civils de Lyon · Updated on 2025-11-21
160
Participants Needed
1
Research Sites
365 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Polycythemia (PG) corresponds to an increase in erythrocyte parameters on a blood test. A distinction is usually made between primary and secondary PG. The most common primary PG is Vaquez's disease, a hematological cancer. In Vaquez disease, an increase in hematocrit has been reported to be associated with a logarithmic increase in blood viscosity. The main complications of primary PGs (especially in Vaquez disease) are thromboembolic complications. In contrast, thromboembolic complications are rarer in secondary PG. In Vaquez disease, a hematocrit ≤ 45% has been defined as the therapeutic goal for significantly reducing thromboembolic risk. However, this has not been established for secondary PGs. All in all, the definition of the 45% threshold is based solely on clinical studies with no obvious biological argument. What's more, simply lowering blood mass through cytoreduction alone does not appear to be sufficient to significantly reduce thromboembolic risk. To investigator knowledge, there are no studies prospectively evaluating blood viscosity, its determinants and coagulation in different types of polycythemia. Nor are there any data on the direct effect on blood viscosity of the various treatments usually offered.
CONDITIONS
Official Title
Blood Viscosity in Polycythemia Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 18 years of age or older
- Followed for a diagnosis or suspicion of polycythemia with hematocrit 2 49% in men and 48% in women
- Affiliated to a social security scheme or similar
You will not qualify if you...
- Therapeutic bloodletting within 3 months prior to inclusion or started cytoreductive therapy before inclusion
- Any other disease or condition likely to change blood viscosity at the investigator's discretion
- Participation in another interventional research protocol that may interfere with this study
- Under guardianship, curatorship, or legal protection
- Under psychiatric care
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Service d'hématologie, Hôpital Lyon Sud
Pierre-Bénite, Lyon, France, 69495
Actively Recruiting
Research Team
M
Mael HEIBLIG, MD,PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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