drugset / Trial / NCT03674658

Propafenone in the Treatment of Atrial Fibrillation

NCT03674658

Completed 71 enrolled TSH Biopharm Corporation Limited
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a open label randomized, multi-center study conducted in Taiwan. The study aims to evaluate the effectiveness and safety of oral Rhynorm (A drug) and Rytmonorm (B drug) for the conversion of paroxysmal AF and is designed to evaluate the improvement in sinus rhythm restoration after the treatment with Rhynorm (A drug) and Rytmonorm (B drug) for 24 weeks.

Timeline

Start
2019-07-11
Primary completion
2021-08-17
Completion
2021-08-17

Drugs

EvaluationDrugModalityDoseRoute
Subject propafenone Unknown Oral

Indications