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| Sponsor: | Procter and Gamble |
|---|---|
| Information provided by: | Procter and Gamble |
| ClinicalTrials.gov Identifier: | NCT00035490 |
Purpose
Implantable cardioverter defibrillators (ICDs) have been developed to treat ventricular tachycardia or fibrillation (abnormal heart rhythms) by electrical shock or by pacing the heart. ICD therapy is established as highly effective for stopping life-threatening arrhythmias, but it does not preclude the use of anti-arrhythmic drugs for prevention and to decrease the frequency of ICD shocks.
The safety and effectiveness of oral azimilide dihydrochloride in reducing the frequency of ICD shocks has been investigated previously in a placebo-controlled study in patients with ICDs. These results need to be confirmed in this larger double-blind, placebo-controlled study with approximately 600 patients.
| Condition | Intervention | Phase |
|---|---|---|
|
Arrhythmia |
Drug: Azimilide Dihydrochloride Drug: placebo |
Phase III |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Double Blind (Subject, Investigator), Placebo Control, Parallel Assignment, Efficacy Study |
| Official Title: | Efficacy and Safety Evaluation of Azimilide Dihydrochloride in Patients With Implantable Cardioverter Defibrillators |
| Enrollment: | 633 |
| Study Start Date: | September 2001 |
| Study Completion Date: | April 2004 |
| Primary Completion Date: | April 2004 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
1: Placebo Comparator
Placebo tablets
|
Drug: placebo
placebo tablet, once daily for one year
|
|
2: Experimental
75 mg azimilide
|
Drug: Azimilide Dihydrochloride
75 mg azimilide, once a day for one year
|
|
3: Experimental
125 mg azimilide
|
Drug: Azimilide Dihydrochloride
125 mg azimilide, once a day for one year
|
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion criteria:
Exclusion criteria:
Contacts and Locations
Show 142 Study Locations| Study Director: | Jose M Brum, MD | Procter and Gamble |
More Information
| Responsible Party: | Procter & Gamble Pharmaceuticals ( Jose Brum, MD ) |
| Study ID Numbers: | 2000098 |
| Study First Received: | May 3, 2002 |
| Last Updated: | July 17, 2009 |
| ClinicalTrials.gov Identifier: | NCT00035490 History of Changes |
| Health Authority: | United States: Food and Drug Administration |
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Membrane Transport Modulators Pathologic Processes Heart Diseases Molecular Mechanisms of Pharmacological Action Therapeutic Uses Calcium Channel Blockers |
Cardiovascular Diseases Cardiovascular Agents Anti-Arrhythmia Agents Pharmacologic Actions Azimilide Arrhythmias, Cardiac |