Clinical Trial

Vietnamese Rapid Acceleration Protocol for Intensifying Drug Therapy in Heart Failure With Reduced Ejection Fraction

Study acronym: VN-RAPID
Recruiting
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Summary
VN-RAPID is an open-label, multicenter, randomized controlled trial evaluating the safety and efficacy of in-hospital initiation and rapid up-titration of four-pillar therapy for hospitalized Asian patients with acute heart failure (AHF) and reduced ejection fraction (HFrEF). The study compares a standardized protocol of intensified treatment (high-intensity care arm) with usual care in patients with elevated NT-proBNP levels who are not on optimal HFrEF medications. The high-intensity care arm involves initiation of all four pillars of HFrEF therapy (RAS inhibitor, beta-blocker, MRA, and SGLT2i) before discharge, followed by a structured 6-week outpatient up-titration process with frequent follow-ups. The study aims for 75% of target doses for RAS inhibitors and beta-blockers, considering the lower blood pressure tendency in Asian populations. Participants will be followed for 180 days to assess clinical outcomes.
Protocol Amendment History 3 amendments
This ClinicalTrials.gov record has been amended 3 times since 2024-09-10; most recent amendment 2025-07-31.
Status change: Not Yet Recruiting → Recruiting 2025-07-31
Trial Details
NCT Number NCT06595290
Lead Sponsor University Medical Center Ho Chi Minh City (UMC)
Collaborators: Momentum Research, Inc., INSERM UMR-942, Paris, France, University of Medicine and Pharmacy at Ho Chi Minh City
Conditions Acute Heart Failure (AHF), Acute Heart Failure With Reduced Ejection Fraction
Enrollment 500 participants
Start Date 2025-08-01
Primary Completion 2028-08-01 (estimated)
Study Completion 2029-01-01 (estimated)
Updated on ClinicalTrials.gov 2025-08-05