Actively Recruiting

Age: 18Years +
All Genders
NCT06421025

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Trial Site Locations

Total: 1 location

1

Service d'hématologie, Hôpital Lyon Sud

Pierre-Bénite, Lyon, France, 69495

Actively Recruiting

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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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