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
| Type | Name | Description |
|---|---|---|
| DRUG | Benzydamine Hydrochloride 0.15% Oral Rinse | Benzydamine Hydrochloride 0.15% Oral Rinse was used to gargle prior to Endoscopic Retrograde Cholangiopancreatography (ERCP) procedure. |
| DRUG | Water | Water 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.