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OpenTrials
Completed

NCT Number: NCT00035464

Efficacy and Safety of Azimilide in the Prophylactic Treatment of Patients With Atrial Fibrillation.

Atrial fibrillation (an abnormal rhythm in the upper chamber of the heart) is a common supraventricular arrhythmia (a type of abnormal heart rhythm) for which antiarrhythmic therapy is often prescribed. The primary goals of therapy are to maintain sinus rhythm (normal heart rhythm) and to reduce the occurrence of episodes of atrial fibrillation. Azimilide may have an effect on increasing the time to first recurrence of symptomatic atrial fibrillation or atrial flutter and symptomatic paroxysmal supraventricular tachycardia (other types of abnormal heart rhythms).

This double-blind, placebo-controlled study is designed to evaluate the efficacy and safety of azimilide compared with placebo in prolonging the time to the first symptomatic arrhythmia recurrence in patients with a history of atrial fibrillation and congestive heart failure and/or ischemic heart disease) and those without these conditions. Once this phase of the study is completed, a second phase with a different study design will be conducted. The second phase is an open-label, follow-up phase. The follow-up phase of the study is designed to evaluate the long-term efficacy and safety of a daily oral dose of azimilide in patients who complete the double-blind, placebo-controlled phase of this study.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Heart Health Institute, Calgary, Alberta, Canada

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • History of symptomatic atrial fibrillation that significantly disrupts the patient's customary daily living activities
  • History of congestive heart failure and/or ischemic heart disease
  • Sinus rhythm (normal heart rhythm) upon entry to the 30 day screening period for the study
  • At least one episode of symptomatic atrial fibrillation during the screening period, with a spontaneous return to sinus rhythm.
  • Sinus rhythm immediately prior to dosing

Exclusion criteria

  • Previously unsuccessful cardioversions within 60 days of screening period
  • Failed to respond to any Class III antiarrhythmic drugs
  • Qualifying arrhythmia due to acute reversible illness, acute myocardial infarction, and/or cardiac or thoracic surgery within one month prior to randomization
  • Previously in an azimilide study

Treatment and study plan

Azimilide Dihydrochloride

Drug

125 mg azimilide tablets, twice a day for 6 months

Placebo

Drug

placebo tablets, twice a day for 6 months

Primary outcomes

  1. To prolong the tachycardia-free period in patients

    Time frame: 6 months

Sponsors and collaborators

Lead sponsor

Forest Laboratories

Industry

Registry information

Official study title

Efficacy and Safety of Azimilide in the Prophylactic Treatment of Patients

Important dates

Study start
2000
Primary completion
2004
Study completion
2004
First posted
May 6, 2002
Registry last updated
Oct 3, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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