Canadian EdoxAban (Lixiana®) Registry in Patients With ATrial Fibrillation and/or ATrial Flutter With Confirmed ValvUlar HeaRt DiseasE (CAPTURE)

Status: Completed
Location: See all (9) locations...
Intervention Type: Drug
Study Type: Observational
SUMMARY

The objective of this registry is the characterization of patients with atrial fibrillation (AF) and/ or atrial flutter (AFL) with confirmed VHD who are prescribed edoxaban in a real life clinical setting.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Male and female patients aged ≥ 18 years at baseline (signing of consent);

• Willing and able to provide written informed consent;

• Patient diagnosed or confirmed with AF and/or AFL within the last 12 months of signed consent form;

• Patient with VHD confirmed by echocardiography within the last 36 months of signed consent form except for mitral stenosis that must be confirmed within the last 12 months;

• Patient at risk for stroke in whom a long term oral anticoagulation is indicated and who are prescribed edoxaban.

Locations
Other Locations
Canada
CIUSSS de l'Estrie-CHUS-Centre Haute-Yamaska-hôpital de Granby
Granby
CISSS de la Montérégie Centre
Greenfield Park
CISSS de Laval
Laval
Montreal Heart Institute
Montreal
IUCPQ
Québec
CISSS du Bas-Saint-Laurent/Hôpital Régional de Rimouski
Rimouski
CISSS de Chaudière-Appalaches - Hopital Saint-Georges
Saint-georges
Centre Hospitalier Universitaire de Sherbrooke
Sherbrooke
CIUSSS de la Mauricie-et-du-Centre-du-Québec
Trois-rivières
Time Frame
Start Date: 2019-04-30
Completion Date: 2025-04-03
Participants
Target number of participants: 136
Treatments
Atrial Fibrillation and/or Atrial Flutter
Subjects taking edoxaban 30mg or 60 mg will be followed for 2 years. Subjects will perform the Montreal Cognitive Assessment (MoCA) Test at baseline and 1-year follow up. They will also answer the Anti-Clot Treatment questionnaire (ACTS-Q) at 1-year.
Authors
Related Therapeutic Areas
Sponsors
Collaborators: Servier
Leads: Montreal Heart Institute

This content was sourced from clinicaltrials.gov