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Benzydamine Hydrochloride Gargle in Reducing Propofol for ERCP — ERCP  

ERCP Clinical Trial

Official title:
Effectivity of Benzydamine Hydrochloride Gargle to Reduce Propofol Consumption in Endoscopic Retrograde Cholangiopancreatography Procedure

Clinical Trial Summary

It was a study aimed to determine the effectivity of benzydamine hydrochloride gargling in reducing propofol consumption in the Endoscopic Retrograde Cholangiopancreatography (ERCP) procedure.

Clinical Trial Description

The study was approved by Ethics Committee of Indonesia University. It was a single-blind randomized clinical trial at Cipto Mangunkusumo Hospital - Jakarta during August to September 2018. 72 subjects were recruited and randomly assigned into 2 groups. Patients in group B were given 0.15% mouthwash with benzydamine hydrochloride prior to procedure while patients in group C were given mouthwash with 15 ml of water. Cumulative propofol consumption per minute per kg body weight, and incidence of postoperative sore throat were measured for each group. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04167592
Study type Interventional
Source Indonesia University
Contact
Status Completed
Phase N/A
Start date August 1, 2018
Completion date October 1, 2018
View Details
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