Clinical Trial

Dalargin for Prevention of Organ Disfunction in High-Risk Abdominal Surgery

Study acronym: Dal-PROTECT
Active, Not Recruiting Phase 3
View on ClinicalTrials.gov →
Record status
This record was last updated February 11, 2026 (before its estimated July 20, 2026 completion). Its status may not reflect the trial's current state.
Summary
Major abdominal surgeries (e.g., gastrectomy, pancreatectomy, colectomy) carry a high risk of life-threatening postoperative complications, including multiorgan disfunction syndrome (MODS), acute kidney injur (AKI), miocardial injury after non-cardiac surgery (MINS) and severe infections. These complications are driven by ischemia-reperfusion injury, leading to oxidative stress and a systemic inflammatory response. Despite advances in surgical and anesthetic techniques, there are no effective pharmacological strategies for personalized prevention of these events, which adversely affect recovery and survival. In this context, opioid receptor agonist, particularly senthetic analogs of Leu-enkephalin such as Dalargin, have emerged as promising agents for pharmacologica preconditioning. Preclinical evidence suggests their ability to mitigate oxidative stress and inflammation by moduating key signaling pathways . The potential for these peptides to protect andothelial function and reduce organ damage presents a novel therapeutic avenue. This study aims to clinically test the hypothesis that perioperative intravenous infusion of Dalargin reduce the incidence and severity of postoperative organ dysfunction. Patients undergoing high-risk abdominal surgery will be randomized to receive either a 72-hour continuous of Dalargin (following a defined dosage regimen) or an identical placebo infusion. the study will also integrate an assessment of genetic polymorphism ( e.g., in NRF2, OLR1, TLR9 genes) to explore personalized approaches to risk stratification and prevention.
Trial Details
NCT Number NCT07404358
Lead Sponsor Botkin Hospital
Conditions Postoperative Complications, Multiple Organ Failure, Abdominal Surgery
Enrollment 200 participants
Start Date 2025-05-13
Primary Completion 2026-07-20 (estimated)
Study Completion 2026-12-20 (estimated)
Updated on ClinicalTrials.gov 2026-02-11