Actively Recruiting

Phase 1
Phase 2
Age: 18Years - 120Years
All Genders
NCT05194111

Treating Heart Dysfunction Related to Cancer Therapy With Sacubitril/Valsartan

Led by Virginia Commonwealth University · Updated on 2026-03-13

53

Participants Needed

1

Research Sites

329 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

To determine feasibility of recruitment and tolerability of treatment with sacubitril-valsartan among adult age survivors of cancer diagnosed at or before age 39 who have stage B heart failure.

CONDITIONS

Official Title

Treating Heart Dysfunction Related to Cancer Therapy With Sacubitril/Valsartan

Who Can Participate

Age: 18Years - 120Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 39 years or younger at the time of cancer diagnosis
  • Clinical records sufficient to confirm diagnosis and treatment
  • Previous treatment with anthracycline chemotherapy
  • Global longitudinal strain less than 18% and/or left ventricular ejection fraction below normal but 40% or higher on echocardiogram or cardiac MRI
  • No symptoms of heart failure (no undue fatigue, palpitations, or shortness of breath during normal activity)
Not Eligible

You will not qualify if you...

  • Age under 18 years
  • Unable to provide consent or have a legally authorized representative
  • Active psychiatric illness that may affect study compliance
  • Limited English or Spanish proficiency that may affect understanding or safety
  • Participation in another intervention study within 30 days or recent investigational drug use
  • More than mild mitral or aortic valve disease before cancer therapy
  • Severe kidney disease (GFR below 30 mL/min/1.73m2)
  • Chronic high potassium levels (above 5 mmol/L)
  • Recent COVID-19 infection or exposure
  • More than moderate tricuspid or pulmonary valve disease before cancer therapy
  • Significant congenital heart disease excluding minor defects
  • More than moderate pericardial effusion
  • Diagnosed constrictive cardiomyopathy before cancer therapy
  • Family history of genetic cardiomyopathy
  • Evidence of infiltrative cardiomyopathy
  • Symptomatic heart disease by NYHA classification
  • Allergy to valsartan or sacubitril
  • Unable to complete cardiac MRI or 6-minute walk test
  • Unable to measure blood pressure and heart rate at home
  • Pregnant or lactating
  • Severe allergic reactions to gadolinium contrast (imaging without contrast may be done)
  • Use of ACE inhibitors, ARBs, aliskiren, NSAIDs, or lithium that cannot be stopped for the study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Virginia Commonwealth University

Richmond, Virginia, United States, 23298

Actively Recruiting

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Research Team

M

Massey CTO CPC Team

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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Treating Heart Dysfunction Related to Cancer Therapy With Sacubitril/Valsartan | DecenTrialz