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Health Status After Switching Angiotensin-converting Enzyme Inhibitors or Angiotensin Receptor Blockers to Sacubitril-valsartan in Patients With Heart Failure With Reduced Ejection Fraction From Rural Tanzania: An Interventional Study

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

Angiotensin-neprilysin inhibitors (ARNI) are beneficial in patients with heart failure with reduced ejection fraction. No study evaluating ARNI has been conducted in sub-Saharan Africa (except South Africa) yet, where heart failure is a major health problem. Before implementing ARNI in Tanzania, a study evaluating the benefit and safety of ARNI in Africans is needed. The aim of this interventional pre-post study is to evaluate the health status of symptomatic patients with heart failure with reduced ejection fraction who are under a chronic heart failure therapy, before and after switching angiotensin converting enzyme (ACE) inhibitors or angiotensin receptor blockers (ARB) to ARNI. Participants will be recruited at the Heart and Lung Clinic of the St Francis Regional Referral Hospital in Ifakara in rural Tanzania during a study period of 30 months, including 10 months of follow-up. A total of 298 participants will be included. The investigators hypothesize that health status, expressed by the Kansas City Cardiomyopathy Questionnaire summary score and 6-minute walking test, will improve after switching from ACE-inhibitors or ARB to ARNI. In Tanzania, sacubitril/valsartan is registered under the name Uperio®.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Symptomatic heart failure NYHA class II-IV and

• Left ventricular ejection fraction (LVEF) ≤40% and

• Treatment with an ACE Inhibitor or an ARB, beta-blocker, and spironolactone in recommended dosages for at least 3 months, and

• Adherence to this therapy of at least 80%.

Locations
Other Locations
United Republic of Tanzania
Heart and Lung Clinic, St Francis Regional Referral Hospital, Ifakara, Tanzania
RECRUITING
Ifakara
Contact Information
Primary
Martin Rohacek, PD Dr med
mrohacek@ihi.or.tz
+255625064252
Backup
Samuel S Mutasingwa, MD
ssalvatory@ihi.or.tz
+255757383124
Time Frame
Start Date: 2026-06-30
Estimated Completion Date: 2028-11-30
Participants
Target number of participants: 298
Treatments
Other: Symptomatic adult particiopants with HFrEF, under heart failure therapy
Symptomatic adults with HFrEF, under heart failure medication
Sponsors
Collaborators: Ifakara Health Institute (IHI)
Leads: Martin Rohacek

This content was sourced from clinicaltrials.gov

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