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Effects of VERApamil versus metoprolol to prevent progression from Paroxysmal to persistent Atrial Fibrillatio

Phase 4
Withdrawn
Conditions
atrial fibrillation
atrial rhythm disorder
10007521
Registration Number
NL-OMON44431
Lead Sponsor
Martini Ziekenhuis
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Withdrawn
Sex
Not specified
Target Recruitment
200
Inclusion Criteria

In order to be eligible to participate in this trial, a subject must meet all of the following criteria:
Patients (age >= 18) with symptomatic paroxysmal AF with an indication for rate control medication who participate in the RACE 5 registry. Patients must be able and willing to sign informed consent for the randomised study.

Exclusion Criteria

Exclusion criteria are (history of) persistent AF, previous adverse effects to the study drugs, heart failure with reduced ejection fraction, symptomatic hypotension, atrioventricular conduction disturbance, severe asthma/COPD, history of pulmonary vein isolation (PVI), pregnancy and breastfeeding.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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