Trial intelligence / Profile preview

Sivelestat sodium to prevent postoperative ARDS in perioperative intra-abdominal infection

ChiCTR2600125882Phase 4Recruiting

Sponsor
Peking University People's Hospital
Start
Jun 2026
Modality
Small Molecules
Countries
1
01

Overview

Phase 4, randomised, double-blind trial in Intra-abdominal infection (IAI) and acute respiratory distress syndrome (ARDS) comparing sivelestat sodium with Control: placebo (2 arms). Primary endpoints: Proportion completing ≥144 hours continuous infusion, Treatment-related discontinuation rate and 1 more. Started Jun 2026; status: recruiting.

02

Drugs

sivelestat
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Conditions

Intra-abdominal infection (IAI)acute respiratory distress syndrome (ARDS)

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