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Death, Sudden clinical trials

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NCT ID: NCT00000531 Completed - Clinical trials for Cardiovascular Diseases

Antiarrhythmics Versus Implantable Defibrillators (AVID)

Start date: September 1992
Phase: Phase 3
Study type: Interventional

To evaluate if use of an implantable cardiac defibrillator (ICD) results in reduction in total mortality, when compared with conventional pharmacological therapy, in patients resuscitated from sudden cardiac death who are otherwise at very high risk of mortality from arrhythmic causes.

NCT ID: NCT00000526 Completed - Clinical trials for Cardiovascular Diseases

Cardiac Arrhythmia Suppression Trial (CAST)

Start date: August 1986
Phase: Phase 3
Study type: Interventional

To determine whether drug treatment of asymptomatic ventricular arrhythmias in post-myocardial infarction patients reduced the incidence of sudden cardiac death and total mortality.

NCT ID: NCT00000525 Completed - Hypertension Clinical Trials

Diuretics, Hypertension, and Arrhythmias Clinical Trial

Start date: July 1986
Phase: Phase 3
Study type: Interventional

To determine whether hypertensive patients with ECG abnormalities and receiving hydrochlorothiazide diuretics were at increased risk of sudden death.

NCT ID: NCT00000518 Completed - Clinical trials for Cardiovascular Diseases

Electrophysiologic Study Versus Electrocardiographic Monitoring (ESVEM)

Start date: July 1985
Phase: Phase 3
Study type: Interventional

To determine whether electrophysiologic study (EPS) or Holter monitoring (HM) was the better method for selecting effective long-term antiarrhythmic drug therapy in patients with sustained ventricular tachycardia, ventricular fibrillation, or an episode of aborted sudden death.

NCT ID: NCT00000492 Completed - Clinical trials for Cardiovascular Diseases

Beta-Blocker Heart Attack Trial (BHAT)

Start date: September 1977
Phase: Phase 3
Study type: Interventional

To determine whether the regular administration of the beta-blocker drug propranolol to people who had had at least one documented myocardial infarction would result in a significant reduction of mortality from all causes over the follow-up period. Eligible volunteer patients were recruited to participate in a double-blind clinical trial within 21 days after the onset of the acute event. One-half of the patients were randomly assigned to a beta-blocking drug (propranolol) and one-half to a placebo. The trial also evaluated the effect of propranolol on incidences of coronary heart disease mortality, sudden cardiac death, and nonfatal myocardial infarction plus coronary heart disease mortality in persons with documented previous myocardial infarction.

NCT ID: NCT00000480 Completed - Clinical trials for Cardiovascular Diseases

Multicenter Unsustained Tachycardia Trial (MUSTT)

Start date: September 1991
Phase: Phase 3
Study type: Interventional

To determine the value of electrophysiologic (EP)-guided antiarrhythmic therapy in coronary heart disease patients at increased risk for sudden death. The study included a controlled clinical trial and a registry.