Clinical Trial

VAPorized Administration of Bumetanide for Outpatient Relief in Heart Failure

Study acronym: VAPOR-HF
Withdrawn Phase 4
View on ClinicalTrials.gov →
Why the trial stopped
Change in Sponsor
Summary
This trial is seeking to determine whether a single 4mg intranasal dose of bumetanide acutely reduces pulmonary artery pressure and blood volume in the outpatient setting for patients with heart failure and an implanted device for remote patient monitoring (i.e. Cordella or CardioMEMS).
Trial Details
NCT Number NCT07375212
Lead Sponsor Prisma Health-Upstate
Conditions Heart Failure Congestive
Start Date 2026-01-21
Primary Completion 2026-01-21 (estimated)
Study Completion 2026-01-21 (estimated)
Updated on ClinicalTrials.gov 2026-01-29