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NCT02832089 Clinical Trial

Oral Carvedilol in Escalating Doses in the Acute Treatment of Atrial Fibrillation

Atrial Fibrillation Clinical Trial

Official title:
Oral Carvedilol in Escalating Doses in the Acute Treatment of Atrial Fibrillation

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02832089
Other study ID # 01AMCRVC
Secondary ID
Status Completed
Phase Phase 3
First received December 28, 2015
Last updated July 11, 2016
Start date December 2000
Est. completion date March 2002

Study information
Verified date July 2016
Source Andhra Medical College
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

Oral carvedilol administered in escalating doses in patients with atrial fibrillation among patients with AF with fast ventricular rate.

Description:

Patients with AF with FVR of any etiology were evaluated and given escalating doses of oral carvedilol in doses - 3.125mg OD, then 3.125 bid, then 6.25mg bid, then 12.5mg bid. The ECG was recorded regularly and analysed for rate reduction or control.

Recruitment information / eligibility
Status Completed
Enrollment 30
Est. completion date March 2002
Est. primary completion date March 2002
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- AF with fast ventricular rate

Exclusion Criteria:

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Drug:
• oral carvedilol
oral carvedilol in escalating doses for reducing ventricular rate in AF patients

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Andhra Medical College

Outcome
Type Measure Description Time frame Safety issue
Primary reduction in ventricular rate in AF patients reduction in ventricular rate in patients with AF and fast ventricular rate. 24 hours Yes
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