Patient Participation
Conditions
Brief summary
The study aims to evaluate the effectiveness and safety of oral fixed-dose combination of bisoprolol/perindopril in patients with permanent atrial fibrillation
Interventions
DRUGperindopril-bisoprolol
outpatients with permanent atrial fibrillation and with preserved ejection fraction
Sponsors
Aversi Clinic
Study design
Observational model
CASE_ONLY
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No
Inclusion criteria
permanent atrial fibrillation with normal EF -
Exclusion criteria
AF with decreased EF \-
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 12-ecg and echocardiography evaluation after 1 month treatment | 1 month |
Countries
Georgia
Outcome results
None listed