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Spironolactone for Paroxysmal Atrial Fibrillation

Not Applicable
Conditions
Atrial Fibrillation
Interventions
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
GroupInterventionDescription
ExperimentalPlaceboDrug intervention
IIISpironolactonePlacebo
ExperimentalSpironolactoneDrug intervention
Primary Outcome Measures
NameTimeMethod
time to a first electrocardiographically confirmed AF3 months
Secondary Outcome Measures
NameTimeMethod
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

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