Not Yet RecruitingPhase 3Phase 4ACTRN12610000753055

A randomised cross-over study of effects of vasodilator treatment on left ventricular mass and volume in patients with chronic aortic regurgitation


Sponsor

National Heart Foundation of NZ

Enrollment

25 participants

Start Date

Oct 1, 2010

Study Type

Interventional

Conditions

Summary

The aim of this study is to determine whether vasodilators, a type of blood pressure treatment, will improve heart function in persons with leaking of the aortic valve. Our hypothesis is that lowering blood pressure will reduce the work of the heart, and over time the volume and thickness of the muscle of the heart's main pumping chamber will improve.


Eligibility

Sex: Both males and femalesMin Age: 18 YearssMax Age: 75 Yearss

Inclusion Criteria1

  • Moderate or severe asymptomatic aortic regurgitation

Exclusion Criteria4

  • current indication for aortic valve replacement
  • other clinically significant cardiac disease
  • contraindication to cardiac magnetic resonance imaging
  • atrial fibrillation

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Interventions

Open label oral vasodilator treatment with dose adjusted according to blood pressure and patient tolerance. Perendopril (2 to 8mg daily) candesartan (4 to 32 mg daily)and/or amlodipine (2.5 to 10mg d

Open label oral vasodilator treatment with dose adjusted according to blood pressure and patient tolerance. Perendopril (2 to 8mg daily) candesartan (4 to 32 mg daily)and/or amlodipine (2.5 to 10mg daily). Either one or a combination of these treatments will be administered to achieve a reduction in blood pressure and adjusted according to tolerance and blood pressure, and continued for one year


Locations(1)

New Zealand

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