Administration of direct oral anticoagulants in patients with myeloproliferative neoplasms.
Jean-Christophe Ianotto, Marie-Anne Couturier, Hubert Galinat...
https://pubmed.ncbi.nlm.nih.gov/28623609/Actively Recruiting
Led by University Hospital, Brest · Updated on 2024-08-12
1000
Participants Needed
1
Research Sites
N/A
Total Duration
This observational study includes patients diagnosed or followed at Brest University Hospital with Philadelphia negative myeloproliferative neoplasms, specifically polycythemia vera, essential thrombocythemia, and primary myelofibrosis. The study aims to collect and analyze clinical and biological data from diagnosis through ongoing follow-up to better understand disease progression and outcomes. Clinical information gathered includes patient and disease characteristics at diagnosis, mutational status, cardiovascular risk factors, and history of thrombosis or cancer. Biological data such as hemogram and bone marrow results are recorded when available. During follow-up, treatment changes and their reasons, thrombotic events, phenotypic changes, and deaths with their causes are noted. Participants are observed until the last update, such as death or change of care center. The main outcome measured is overall survival over 10 years, with secondary outcomes including incidence of disease evolutions and thromboses over the same period. Patients who are alive are asked to sign a consent form to continue in the study.
CONDITIONS
Myeloproliferative Neoplastic Diseases Observatory From Brest
J
Jean-Christophe Ianotto
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University Hospital, Brest
Lead Sponsor
You may qualify if you...
You will not qualify if you...
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 10 years
Participants who undergo routine care are observed over time with clinical and biological data collected from diagnosis until last news.
Visits as per routine healthcare and follow-up
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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Lead Sponsor