RecruitingPhase 3NCT05198960
AVAJAK: Apixaban/Rivaroxaban Versus Aspirin for Primary Prevention of Thrombo-embolic Complications in JAK2V617F-positive Myeloproliferative Neoplasms
Studying Essential thrombocythemia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- University Hospital, Brest
- Intervention
- Direct Oral Anticoagulants(drug)
- Enrollment
- 1308 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2022 – 2027
Study locations (30)
- CHU d'Angers, Angers, France
- CH d'Annecy, Annecy, France
- CH d'Argenteuil, Argenteuil, France
- CH d'Avignon, Avignon, France
- CH de la Côte Basque Bayonne, Bayonne, France
- CH de Béziers, Béziers, France
- CHU Bordeaux, Bordeaux, France
- CHU Brest, Brest, France
- Hôpital privé Cesson-Sévigné, Cesson-Sévigné, France
- CHU de Clermont-Ferrand, Clermont-Ferrand, France
- Hôpital Henri Mondor (APHP), Créteil, France
- CHU Grenoble Alpes, Grenoble, France
- CHD Vendée La Roche Sur Yon, La Roche-sur-Yon, France
- CHU Le Havre, Le Havre, France
- CH Le Mans, Le Mans, France
- +15 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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