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

Outcome

Met primary endpoint

paper This finding indicates that Rhynorm is not inferior to Rytmonorm ( p = 0.023 for noninferiority). PMID 36800262 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject propafenone Unknown — Oral

Indications