Atrial Fibrillation Feasibility Certoparin Trial - AFFECT
Completed · Phase 3
Conditions studied: Persistent Nonvalvular Atrial Fibrillation
In brief
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
Key facts
- Study ID
- NCT00171769
- Run by
- Novartis
- People needed
- 200
- Starts
- 2005-04-01
- Last updated by the study team
- 2017-02-23
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- persistent AF (electrical cardioversion is planned)
- written informed consent
You may not qualify if…
- acute clinical signs of venous thromboembolism
- current oral anticoagulation
- indication for medical cardioversion
Where it is running
- Novartis Pharmaceuticals — East Hanover, New Jersey, United States
- Study site — Investigative Centers, Germany
Full record on ClinicalTrials.gov
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