CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 135 enrolled
Drug / intervention
1g of F373280 +1 moredrug
Likely dose
1g of F373280from record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01831856
NCT01831856Phase 2Completed

Efficacy and Safety Study of F373280 for Maintenance of Sinus Rhythm After Electrical Cardioversion in Patients With Persistent Atrial Fibrillation and Chronic Heart Failure. International, Multicentric, Randomised, Double-blind, Placebo Controlled Study.

Pierre Fabre Medicament·interventional·Posted Apr 15, 2013·Updated Jul 2, 2019

In Brief

A Phase 2 clinical trial evaluating 1g of F373280 and Placebo for Atrial Fibrillation. Completed, enrolled 135 participants across 20 sites in 5 countries.

Detailed Summary

The purpose of this study is to assess the efficacy of F373280 on the maintenance of normal cardiac rhythm after direct electric cardioversion in patients with persistent atrial fibrillation and cardiac failure.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCzechia, Hungary, Italy, Poland, Spain
Collaborators--

Timeline

Phase 2CompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedApr 15, 2013
Enrollment StartApr 1, 2013
Primary CompletionApr 3, 2017
Study CompletionJun 21, 2017
TodayJul 2, 2026
Enrollment to primary: 4.0 yearsPosted 13.2 years ago

Interventions

1g of F373280drug

Oral administration, one capsule each evening with dinner.

Placebodrug

Oral administration, one capsule each evening with dinner.