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Clinical Trials/NCT00171769
NCT00171769
Completed
Phase 3

An Open Label, Multi-center Trial to Evaluate the Feasibility and Safety of Short-term Treatment With Subcutaneously Injected Certoparin (8000 U Anti-Xa Twice Daily) in Patients With Persistent Nonvalvular Atrial Fibrillation

Novartis1 site in 1 country200 target enrollmentApril 2005

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Persistent Nonvalvular Atrial Fibrillation
Sponsor
Novartis
Enrollment
200
Locations
1
Primary Endpoint
Safety measures including reporting of serious adverse events and adverse events, including vascular and neurological events
Status
Completed
Last Updated
9 years ago

Overview

Brief 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

Registry
clinicaltrials.gov
Start Date
April 2005
End Date
August 2006
Last Updated
9 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Novartis

Eligibility Criteria

Inclusion Criteria

  • persistent AF (electrical cardioversion is planned)
  • written informed consent

Exclusion Criteria

  • acute clinical signs of venous thromboembolism
  • current oral anticoagulation
  • indication for medical cardioversion

Outcomes

Primary Outcomes

Safety measures including reporting of serious adverse events and adverse events, including vascular and neurological events

Study Sites (1)

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