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Clinical Trials in China / NCT04964869
Recruiting Not applicable

Efficacy of Prophylactic Epinephrine Solution Injection in Prevention of Delayed Post-sphincterotomy

NCT04964869 · tracked via the Priya Life Science China tracker
Sponsor
Wen-Hsin Huang
Phase
Not applicable
Started
2021-07-15
Last updated
2024-10-24

Condition(s) studied

Bleeding Hemorrhage

Investigational drug(s) / intervention(s)

epinephrine solution injection

epinephrine solution injection: epinephrine solution injection at least 1 ml to the post- sphincterotomy wound

Study summary

Bleeding is the most frequently reported serious complication of endoscopic sphincterotomy, and severe bleeding has occurred in about 1% to 2% of patients. Endoscopic injection of epinephrine is the most commonly used, effective, and least expensive method for the management of post- sphincterotomy bleeding. However, the efficacy of prophylactic saline-epinephrine solution injection to prevent delayed EST bleeding when transient bleeding During ERCP has not been established.

Eligibility

Sex
ALL
Min age
20 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * Age 20 years or older. * Ability to give informed consent. * An naive major papilla. * Transient bleeding after endoscopic sphincterotomy * Bleeding less than 30 secs when end of procedure Exclusion Criteria: * Prior endoscopic sphincterotomy. * Thrombocytopenia (platelets \<50,000/mm3). * Liver cirrhosis (Child A-C) * CKD stage 4-5 and dialysis. * Allergy to epinephrine * Prolonged PT/APTT (INR\>1.5) * Had exposure any antithrombotic or antiplatelet agent in recent 7 days and/or will take those agents in one month after EST * Ampulla Vater tumor * Active GI bleeding * Pregnancy * Limited visibility when immediate bleeding after sphincterotomy * Still bleeding after 30 secs when end of procedure * Recurrent bleeding during ERCP

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
China Medical University Hospital Taichung North Dist. Recruiting

More Wen-Hsin Huang trials in China

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04964869 on ClinicalTrials.gov ↗ ← All trials in China