drugset / Trial / NCT06031363

The Optimal Dose of Indomethacin Suppository for Preventing Post-ERCP Pancreatitis

NCT06031363

RandomizedParallel-groupSingle-blindPrevention

Summary

This study is a single-center, randomized, single-blind, parallel controlled clinical study to explore the optimal dose of postoperative indomethacin suppository for the prevention of post-ERCP pancreatitis. The purpose of this study is to explore the optimal dosage of indomethacin suppository for PEP prevention, to study the control effect of indomethacin on hyperamylaseemia, and to further explore the group of patients who benefit most from this therapy.

Timeline

Start
2022-11-01
Primary completion
2023-12-06
Completion
2024-01-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Indomethacin Small molecule 50 mg Rectal
Subject Indomethacin Small molecule 100 mg Rectal
Subject Indomethacin Small molecule 150 mg Rectal

Indications