Angiotensin-II Blockade in Mitral Regurgitation

Mitral Regurgitation Clinical Trial

Official title:

Angiotensin-II Blockade in Mitral Regurgitation

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00587470
• Other study ID #: 1129-98
• Status: Completed
• Phase: Phase 4
• First received: December 21, 2007
• Last updated: October 14, 2010
• Start date: August 1998
• Est. completion date: August 2001

Study information

• Verified date: October 2010
• Source: Mayo Clinic
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

Mitral regurgitation (MR) is common in the elderly and its prevalence is increasing with the aging of the population. Organic MR, due to primary valvular lesions, initiates a cascade of complications determined by its degree. MR of severe degree is associated with excess mortality and high cardiac morbidity (heart failure, atrial fibrillation). It also causes left ventricular remodeling which induces left ventricular dysfunction, which in turn leads to poor clinical outcome. Surgery can eliminate MR, but carries immediate and long-term risks, especially in the elderly. Therefore, chronically decreasing the degree of MR is a major goal of medical therapy but such an effect is yet unproved because of conflicting results of small and mostly non-randomized series. Our recent preliminary studies suggest that a sustained decrease of degree of MR and improvement of left ventricular remodeling can be achieved with powerful reduction of afterload, obtained in particular with angiotensin-II receptor blockade. Therefore, the present proposal seeks to address gaps of knowledge regarding vasoactive treatment of MR through the verification of the following hypothesis: Hypothesis: Vasoactive therapy using angiotensin-II receptor blocker (Candesartan Cilexetil) weighed against placebo produces a sustained reduction of the consequences of organic MR. The specific aims are that the treatment a) decreases the degree of MR (decreases the regurgitant volume, primary end-point) and b) improves left ventricular remodeling (decreases the end-diastolic volume index, secondary end-point), as compared to placebo.

Description:

Patients with MR organic (intrinsic valve disease), isolated (no other valve disease), moderate or more severe (regurgitant volume *30 mL/beat). A Clinical trial, randomized, placebo controlled, double-blind, without cross-over, of 1 year oral treatment with potent angiotensin-II receptor blockade using 32 mg Candesartan daily. The trial is preceded in all patients by an acute open-label study to determine tolerance and immediate response. The methods used to measure the end-points will be: a) Doppler-Echocardiography for quantitation of the degree of MR (measurement of regurgitant volume) using a combination of three simultaneous methods (quantitative Doppler, quantitative two-dimensional echocardiography, proximal flow convergence) and b) of left ventricular remodeling (end-diastolic volume index measured by echocardiography and by electron beam computed tomography). This single center study seeks to enroll a total of 90 patients. The analysis will be based on intention to treat and compare the regurgitant volume and left ventricular end-diastolic volume index measured after one year of treatment with the active drug or placebo. The results of the trial should provide strong evidence regarding medical treatment of patients with organic MR.

Other known NCT identifiers

• NCT00014846

Recruitment information / eligibility

• Status: Completed
• Enrollment: 60
• Est. completion date: August 2001
• Est. primary completion date: August 2001
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

Patients:

• 18 years old or older, with

• Mitral regurgitation on the basis of Color flow imaging

• Due to organic disease of the mitral valve on the basis of two-dimensional echocardiography

• Isolated (no valve disease other than functional tricuspid regurgitation on the basis of Doppler-Echocardiography)

• Pure (no mitral stenosis by Doppler echocardiography)

• Quantifiable by Doppler-Echocardiographic methods

• Of more than mild degree, defined as regurgitant volume * 30 mL/beat

• Occurring on native valves

• With Two-dimensional echocardiographic imaging allowing assessment of LV remodeling, and

• Asymptomatic (or mildly symptomatic but not considered as candidates for immediate surgery by their attending physician).

Exclusion Criteria:

• Associated aortic valve disease (more than trace aortic regurgitation by color flow imaging or mean gradient *25 mmHg)

• Associated mitral stenosis (mean gradient* 5 mmHg, valve area < 1.5 cm2)

• Associated congenital or pericardial diseases on the basis of Doppler echocardiography

• Intolerance to either AII blockers or Angiotensin converting enzyme inhibitors

• Intolerance to iodine contrast material

• Intolerance to intravenous echographic contrast agents

• Renal failure with creatinine * 2 mg/dl

• Blood pressure below 100 mmHg

• Known renal artery stenosis

• Ongoing therapy with hydralazine, calcium-entry blocking drugs or angiotensin converting enzyme inhibitors

• Known severe comorbidity such as liver disease, malignancy

• Pregnancy (A negative pregnancy test and effective contraceptive methods are required prior to enrollment of females of childbearing potential (not post-menopausal or surgically sterilized)), and

• Patients considered as requiring mitral valve surgery by their attending physician or with previous valve repair or replacement.

Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Mitral Regurgitation
• Mitral Valve Insufficiency

Intervention

Drug:
• Candesartan
Maximum vasodilation.
• atacand
maximum vasodilation
• Placebo
Placebo

Locations

Country	Name	City	State
United States	Mayo Clinic	Rochester	Minnesota

Sponsors (1)

Lead Sponsor	Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Tolerance of the medication.		one year	Yes
Secondary	Decrease of severity of mitral regurgitation.		1 year	No