Clinical Trials Directory

Trials / Completed

CompletedNCT02862366

Role of the Circulating Procoagulants Microparticles in the Hypercoagulability of MNP Ph1-

Role of the Circulating Procoagulants Microparticles in the Hypercoagulability of Chronic Philadelphia Negative Myeloproliferative Neoplasms

Status
Completed
Phase
Study type
Observational
Enrollment
128 (actual)
Sponsor
Lille Catholic University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

Patients with myeloproliferative neoplasms Philadelphia chromosome negative (MPNsPh1-) such as Essential thrombocytosis (ET), Polycythemia vera (PV) and Primary Myelofibrosis (PMF) have a higher risk of arterial or deep-vein thrombosis. This is responsible for a significant increase in mortality (up to 31% of increase in thrombosis risk in ET). Cellular inflation and blood hyperviscosity, resulting from these diseases, fail to account for these thromboses, as more than 50% of thrombotic complications happen under adapted antineoplastic drug treatment. These last years, cellular microparticles (MPs) have been shown to play a major role in thrombogenesis. MPs are generated by apoptosis or the activation of malignant cells, platelets, endothelial cells or monocytes. They are fragments of plasma membrane, smaller than 1 µm, rich in phosphatidylserine, which can express the tissue factor and serve as support for the coagulation factors. Increase in the plasma concentration of procoagulant platelet microparticles has been demonstrated in other thrombotic diseases (acute coronary syndrome, disseminated intravascular coagulation DIC, etc.). The working hypothesis is that platelet microparticles are involved in the hypercoagulability of MPNs patients.

Conditions

Interventions

TypeNameDescription
OTHERBlood samplingBlood sampling every 6 month following the routine calendar of visit

Timeline

Start date
2010-10-01
Primary completion
2016-01-25
Completion
2016-01-25
First posted
2016-08-11
Last updated
2018-10-31

Locations

3 sites across 1 country: France

Source: ClinicalTrials.gov record NCT02862366. Inclusion in this directory is not an endorsement.