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NCT03488420Completed

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

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

Source: ClinicalTrials.gov · Last updated 6 Apr 2025

Brief summary (registry, in English)

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.

Status (registry)
Completed
Study type
Observational
Enrollment
136 (actual)
First submitted
20 Mar 2018
Start date
30 Apr 2019
Primary completion date
21 Mar 2025
Lead sponsor
Montreal Heart Institute
NCT number
NCT03488420

What you commit to

  • Study type: Observational
  • Participants enrolled: 136
  • From 30 Apr 2019 to the primary completion date, 21 Mar 2025
  • 9 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Patients with a mechanical heart valve or rheumatic mitral stenosis, or moderate and severe non rheumatic mitral stenosis;
  • Patients planned to have an intervention for valvular heart disease in the next 12 months;

Other

  • Patients with AF and/or AFL secondary to reversible cause;
  • Pregnant or breastfeeding women.
  • Short term anticoagulation post cardioversion or ablation.

Who the study is looking for

  • 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.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (9)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
CIUSSS de l'Estrie-CHUS-Centre Haute-Yamaska-hôpital de Granby
Coordinator of this site? Confirm its status
GranbyCanadaUnknown status
CISSS de la Monteregie-Centre
Coordinator of this site? Confirm its status
Greenfield ParkCanadaUnknown status
CISSS de Laval
Coordinator of this site? Confirm its status
LavalCanadaUnknown status
Montreal Heart Institute
Coordinator of this site? Confirm its status
MontrealCanadaUnknown status
IUCPQ
Coordinator of this site? Confirm its status
QuébecCanadaUnknown status
CISSS du Bas-Saint-Laurent/Hôpital Régional de Rimouski
Coordinator of this site? Confirm its status
RimouskiCanadaUnknown status
CISSS de Chaudière-Appalaches - Hopital Saint-Georges
Coordinator of this site? Confirm its status
Saint-GeorgesCanadaUnknown status
Centre Hospitalier Universitaire de Sherbrooke
Coordinator of this site? Confirm its status
SherbrookeCanadaUnknown status
CIUSSS de la Mauricie-et-du-Centre-du-Quebec
Coordinator of this site? Confirm its status
Trois-RivièresCanadaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.