RecruitingPhase 4NCT06917664

Treatment of Moderate Ischemic Mitral Regurgitation in Patients With Coronary Artery Disease


Sponsor

China National Center for Cardiovascular Diseases

Enrollment

220 participants

Start Date

Jun 5, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

This study aims to evaluate the effect of angiotensin receptor/neprilysin inhibitors (ARNI) on improving ischemic mitral regurgitation (IMR) in patients with coronary artery disease undergoing isolated coronary artery bypass grafting (CABG) through a randomized controlled clincial trial.


Eligibility

Min Age: 18 Years

Inclusion Criteria2

  • Fully informed and voluntarily signed informed consent;
  • Received CABG and moderate IMR was diagnosed on two consecutive preoperative transthoracic echocardiography (according to 2021 ESC/EACTS Guidance Standards )

Exclusion Criteria1

  • Symptomatic hypotension and/or a SBP < 100 mmHg at screening; 2.Estimated GFR < 30 mL/min/1.73m2; 3.Serum potassium > 5 mmol/L at screening; 4.History of angioedema or unacceptable side effects while receiving ACE inhibitors or ARBs; 5.Patients receiving mitral valve intervention at the same time, or have participated in other clinical trials, or are unwilling to participate in this study.

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Interventions

DRUGsacubitril/valsartan

Sacubitril/valsartan therapy after isolated CABG


Locations(1)

China National Center for Cardiovascular Diseases

Beijing, Beijing Municipality, China

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NCT06917664


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