DOAC in Unusual Site Venous Thrombosis

CompletedOBSERVATIONAL
Enrollment

358

Participants

Timeline

Start Date

October 1, 2019

Primary Completion Date

December 31, 2024

Study Completion Date

December 31, 2024

Conditions
Splanchnic Vein ThrombosisCerebral Vein ThrombosisOvarian Vein ThrombosisRenal Vein ThrombosisRetinal Vein Thrombosis
Interventions
DRUG

Direct Oral Anticoagulants

Consecutive adult patients with objectively diagnosed unusual site venous thrombosis and treated with one of the DOAC (e.g. apixaban, dabigatran, edoxaban, rivaroxaban) will be eligible for this observational prospective registry

Trial Locations (24)

48202

Henry Ford Health System, Detroit

Unknown

Ottawa Hospital Research Institute, Ottawa

CHU Amiens Picardie, Amiens

Hôpital de la Cavale Blanche, Brest

Hôpital Edouard Herriot, Lyon

Hopital Louis Mourier, Paris

Hôpital Européen Georges Pompidou, Paris

Centre Hospitalier Universitaire de Saint-Etienne, Saint-Etienne

Sheba medical center, Tel Litwinsky

Azienda Ospedaliera Universitaria di Bologna, Bologna

Ospedale Maggiore, Bologna, Bologna

Ospedale Sant'Anna, ASST Lariana, Como

Ospedale Policlinico San Martino, Genova

Ospedale San Paolo, Milan

University Hospital of Padova, Padua

Catholic University, Rome

Sapienza Università di Roma, Rome

University of Insubria, Varese

University of Malta, Msida

Radboud University Medical Center Nijmegen, Nijmegen

University Medical Centre Ljubljana, Ljubljana

Clinica Universidad de Navarra, Madrid

Virgen del Rocío Hospital and Instituto de Biomedicina, Seville

King Chulalongkorn Memorial Hospital, Bangkok

All Listed Sponsors
collaborator

Università degli Studi dell'Insubria

OTHER

lead

University of Malta

OTHER

NCT03778502 - DOAC in Unusual Site Venous Thrombosis | Biotech Hunter | Biotech Hunter