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The Effect of Perioperative DEXamethasone on Postoperative Complications After PANcreaticoduodenectomy — PANDEX  

Pancreaticoduodenectomy Clinical Trial

Official title:
The Effect of Perioperative DEXamethasone on Postoperative Complications After PANcreaticoduodenectomy

Clinical Trial Summary

The primary objective of this clinical trial is evaluate the effect of dexamethasone on postoperative complications after pancreaticoduodenectomy.

Clinical Trial Description

This is a multicentric, prospective, randomized, double-blind, pragmatic, placebo-control study. Patients who are going to receive elective pancreaticoduodenectomy will be randomized to receive 0.2 mg/kg dexamethasone or saline placebo, administered as an intravenous bolus within 5 minutes after induction of anesthesia. The primary outcome is the Comprehensive Complication Index (CCI) score within 30 days after the operation, which will be compared between these two groups . ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05567094
Study type Interventional
Source Ruijin Hospital
Contact
Status Completed
Phase Phase 4
Start date October 8, 2022
Completion date September 14, 2023
View Details
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