Overview

Response to RSD1235 Compared to Placebo in Subjects With Atrial Arrhythmia After Heart Surgery

Status:
Completed
Trial end date:
2007-02-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to demonstrate the safety and efficacy of RSD1235 compared to placebo in the conversion of atrial arrhythmia to sinus rhythm in subjects following valvular and/or coronary artery bypass graft surgery.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Astellas Pharma Inc
Collaborators:
Astellas Pharma US, Inc.
Cardiome Pharma
Correvio International Sarl
Criteria
Inclusion Criteria:

- Documented atrial arrhythmia after valvular and/or coronary artery bypass graft
surgery

Exclusion Criteria:

- Unstable Class IV heart failure