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Secondary Prevention of Atrial Fibrillation (Impact of Renin-Angiotensin-Aldosterone System Inhibition)

Secondary Prevention of Atrial Fibrillation (Impact of Renin-Angiotensin-Aldosterone System Inhibition)

Status
Terminated
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01233635
Enrollment
228
Registered
2010-11-03
Start date
2005-11-30
Completion date
2007-11-30
Last updated
2023-03-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atrial Fibrillation

Brief summary

In the present application, we propose to refine and extend current insight into AAF mechanism and therapy by examining the importance of pharmacologic RAAS inhibition, ACE genotype, and their interaction in secondary AF prevention. We have 3 specific aims: 1. To confirm that RAAS inhibition therapy reduces the incidence of AF recurrence. 2. To test the hypothesis that the incidence of AF recurrence in the absence of RAAS inhibition therapy is higher among patients with the D allele. 3. To explore the hypothesis that RAAS inhibition therapy is more effective for preventing AF recurrence in patients with the DD genotype than in those with DI or II genotypes.

Interventions

OTHERno drug

none, no drug

DRUGstart cozaar

start cozaar

DRUGcontinue cozaar

continue cozaar

Sponsors

University of Pittsburgh
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Subjects must be in atrial fibrillation confirmed by 12 lead EKG. * blood pressure \> 90 mmHg * Patient without cardiopulmonary symptoms * 18+ years of age

Exclusion criteria

* Contraindiction to warfarin * Recent (within 6 months) MI or cardiac revascularization * Recent (within 6 months) CVA or TIA * NYHA Class IV CHF * Active thyroid disease * Major hepatic dysfunction * Renal dysfunction (\>2 mg/dL) * Hyperkalemia (\>4.6 mEq/L) * Hyponatremia (\<130 mEq/L) * Currently taking a Vaughn-Williams Type I or III antiarrhythmic drug * History of ARB intolerance * Contraindication to ARB therapy * Pregnancy * Female of childbearing age * Age \< 18 years of age * Inability to give informed consent * Other medical conditions calling 1 year survival into question

Design outcomes

Primary

MeasureTime frame
AF burden1 year

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026