Clinical Trials Directory

Trials / Completed

CompletedNCT04167592

Benzydamine Hydrochloride Gargle in Reducing Propofol for ERCP

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
72 (actual)
Sponsor
Indonesia University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
DRUGBenzydamine Hydrochloride 0.15% Oral RinseBenzydamine Hydrochloride 0.15% Oral Rinse was used to gargle prior to Endoscopic Retrograde Cholangiopancreatography (ERCP) procedure.
DRUGWaterWater was used to gargle prior to Endoscopic Retrograde Cholangiopancreatography (ERCP) procedure.

Timeline

Start date
2018-08-01
Primary completion
2018-09-01
Completion
2018-10-01
First posted
2019-11-19
Last updated
2019-11-19

Locations

1 site across 1 country: Indonesia

Source: ClinicalTrials.gov record NCT04167592. Inclusion in this directory is not an endorsement.