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NCT04484688 Clinical Trial

Prestilol(Perindopril+Bisoprolol) in Therapy of Patients With Atrial Fibrilation

Patient Participation Clinical Trial

Official title:
Perindopril+Bisoprolol in Therapy of Patients With Atrial Fibrilation

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT04484688
Other study ID # Prestilol
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date August 1, 2020
Est. completion date December 1, 2021

Study information
Verified date July 2020
Source Aversi Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The study aims to evaluate the effectiveness and safety of oral fixed-dose combination of bisoprolol/perindopril in patients with permanent atrial fibrillation

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 50
Est. completion date December 1, 2021
Est. primary completion date September 1, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:permanent atrial fibrillation with normal EF -

Exclusion Criteria:AF with decreased EF

-

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• perindopril-bisoprolol
outpatients with permanent atrial fibrillation and with preserved ejection fraction

Locations
Country Name City State
Georgia Aversi Clinic Tbilisi
Georgia Aversi Clinic Tbilisi

Sponsors (1)
Lead Sponsor Collaborator
Aversi Clinic

Country where clinical trial is conducted

Georgia, 

Outcome
Type Measure Description Time frame Safety issue
Primary 12-ecg and echocardiography evaluation after 1 month treatment 1 month
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