Clinical Trials Directory

Trials / Completed

CompletedNCT04586972

Safety and Efficacy of Apixaban in Very Old Geriatric Subjects (> 80 Years) With Atrial FIbrillation in a Prospective reAl World Study;

Status
Completed
Phase
Study type
Observational
Enrollment
977 (actual)
Sponsor
Gérond'if · Academic / Other
Sex
All
Age
80 Years
Healthy volunteers
Not accepted

Summary

The main objective of this study is to realize an observational "real life" study conducted in French geriatric settings, to assess safety and efficacy in ≥ 80 year-old patients with nonvalvular Atrial fibrillation (AF) newly treated with Apixaban. Moreover, in this geriatric population the adequacy of Apixaban dosage and events (bleeding and stroke) will be assessed.

Detailed description

It is a muliticentric, observational, prospective study. This study will be conducted in about 40 geriatric settings in France. The planned duration of the inclusion period is 27 months in each center. The follow-up period starts from inclusion up to one year after inclusion with phone contact or unscheduled visit at 3, 6, 9 and 12 months. During this follow-up, participants physicians will record patients' data during visit directly from the patients or their physicians or their families and by phone. The following data will be colllected: * At M0 : Socio-demographics, clinical and biological data; embolic risk and emorrhagic risk scores,cognitive function, number of falls, blood pressure, nutritional assessment, athonomy, comorbidities, data on anticoagulant therapy, treatment discontinuation and clinical evaluation. * At M3, M6, M9 and M12: • Number of falls, all treatment schedule, record of major bleeding events, record of any other bleeding events, record of other serious events, record of other non-major events, treatment discontinuation, and social and medical environment. * Only M6 and M12: Renal function (both Cockcroft-Gault, chronic Kidney Disease, epidemiology Collaboration "CKD EPI" and the four variable modification of Diet in renal Disease equation "MDRD")

Conditions

Timeline

Start date
2020-09-23
Primary completion
2023-12-21
Completion
2024-04-29
First posted
2020-10-14
Last updated
2025-09-16

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT04586972. Inclusion in this directory is not an endorsement.