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Study identifier: NCT06595290 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

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

Condition: Acute Heart Failure (AHF) · Acute Heart Failure With Reduced Ejection Fraction  ·  Sponsor: University Medical Center Ho Chi Minh City (UMC)

PhaseNA
Planned participants500
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Vu Hoang Vu, Ph.D M.D  ·  +84908431304‬  ·  vu.vh@umc.edu.vn

Nam Thanh Hai Phan, M.D  ·  +84937728990  ·  nam.pth2@umc.edu.vn

Always discuss trial participation with your own doctor first.

Locations (4)

An Giang Heart HospitalLong Xuyen, An Giang, VietnamNot Yet Recruiting
Thong Nhat HospitalHo Chi Minh City, Ho Chi Minh City, VietnamNot Yet Recruiting
University Medical Center Ho Chi Minh CityHo Chi Minh City, Ho Chi Minh City, VietnamRecruiting
Quang Tri Province HospitalĐông Hà, Quang Tri, VietnamNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT06595290