Clinical Trials Directory

Trials / Completed

CompletedNCT00313157

RATe Control in Atrial Fibrillation

Rate Control in Atrial Fibrillation

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
80 (actual)
Sponsor
Asker & Baerum Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to compare the effect of metoprolol, verapamil, diltiazem and carvedilol on ventricular rate, working capacity and quality of life in patients with chronic atrial fibrillation.

Detailed description

This is a randomised, single blinded, cross-over study comparing the efficacy of metoprolol 100 mg o.d., verapamil 240 mg o.d., diltiazem 360 mg o.d. and carvedilol 25 mg o.d. in reducing ventricular rate in atrial fibrillation. A total of 60 patients will be included, with a minimum of 20 women.Patients will receive each of the drug regimens in a random sequence. Each regimen will be administered for 3 weeks, ensuring that steady-state drug concentration will be attained and to provide an adequate washout of the previous treatment. Following each regimen, exercise ECG and Holter registration will be performed and patients will undergo laboratory evaluation and complete QoL-forms. They will then be started on the next randomly assigned treatment regimen, until the entire sequence of treatment schedules is completed.

Conditions

Interventions

TypeNameDescription
DRUGMetoprolol
DRUGDiltiazem
DRUGVerapamil
DRUGCarvedilol

Timeline

Start date
2006-04-01
Primary completion
2010-09-01
Completion
2010-09-01
First posted
2006-04-12
Last updated
2014-05-13

Locations

1 site across 1 country: Norway

Source: ClinicalTrials.gov record NCT00313157. Inclusion in this directory is not an endorsement.