drugset / Trial / NCT00171769

Atrial Fibrillation Feasibility Certoparin Trial - AFFECT

NCT00171769

Phase 3 Completed 200 enrolled Novartis
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This trial is designed to provide data about feasibility and safety of short-term treatment with the low-molecular-weight heparin certoparin in patients with persistent nonvalvular atrial fibrillation

Timeline

Start
2005-04
Primary completion
2006-08
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Certoparin Other / unclassified 8000 iu Subcutaneous