Spironolactone for Paroxysmal Atrial Fibrillation
- Registration Number
- NCT00689598
- Lead Sponsor
- Taichung Veterans General Hospital
- Brief Summary
To determine whether or not spironolactone can prevent or delay the occurrence of atrial fibrillation.
- Detailed Description
To determine whether or not adding spironolactone can prevent or delay the occurrence of paroxysmal atrial fibrillation in patients who have received propafenone treatment.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
Not provided
Exclusion Criteria
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Experimental Placebo Drug intervention III Spironolactone Placebo Experimental Spironolactone Drug intervention
- Primary Outcome Measures
Name Time Method time to a first electrocardiographically confirmed AF 3 months
- Secondary Outcome Measures
Name Time Method 1. Response rate: Improvement of any symptom scores and/or SF36 scores more than 50 % (compared with re-randomization scores) 2. Difference of mean episodes of documented AF between the spironolactone and placebo groups. 3 months
Trial Locations
- Locations (1)
Taichung General Hospital
🇨🇳Taichung, Taiwan