Clinical Trial

Recombinant Human Brain Natriuretic Peptide for the Recovery Stage of Septic Shock

Study acronym: rh-BNP-RSS
Not Yet Recruiting
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Record status
This record was last updated July 29, 2025 (before its estimated June 2026 completion). Its status may not reflect the trial's current state.
Summary
As infection control improves and circulation stabilizes, treatment de-escalation of septic shock begins, accompanied by fluid redistribution from interstitial spaces to the vasculature, increasing cardiac volume load. Synthetic recombinant human BNP (rh-BNP) plays a role in inducing vasodilation, particularly in the venous system, alleviating cardiac congestion, and enhancing natriuresis and diuresis. Thus the investigators designed a single-center, prospective physiological study to evaluate the efficacy of standard rh-BNP infusion in reducing venous return and enhancing fluid removal, with a secondary objective of assessing the maintenance of perfusion pressure and tissue perfusion.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2024-12-17.
Trial Details
NCT Number NCT06745206
Lead Sponsor Sichuan Provincial People's Hospital
Collaborators: Tibet Kangzhe Pharmaceutical Development Co., Ltd
Conditions Sepsis-induced Cardiomyopathy, the Recovery Phase of Septic Shock
Enrollment 30 participants
Start Date 2025-12
Primary Completion 2026-06 (estimated)
Study Completion 2026-09 (estimated)
Updated on ClinicalTrials.gov 2025-07-29