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临床试验/NCT04167592
NCT04167592已完成不适用

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

Indonesia University1 个研究点 分布在 1 个国家目标入组 72 人开始时间: 2018年8月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
72
试验地点
1
主要终点
Cumulative Propofol Consumption

研究概览

简要总结

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

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • undergoing ERCP
  • ASA I-III
  • BMI 18-30 kg/m2

排除标准

  • allergic to propofol
  • contraindicated to propofol
  • had throat wound or laceration
  • received analgesics or steroid in 24 hours priorly
  • unstable during sedation
  • procedure longer than 90 minutes

研究组 & 干预措施

Benzydamine Hydrochloride Group

Active Comparator

Subjects who were allocated in benzydamine group would gargle with 15 of ml benzydamine hydrochloride 0.15% before sedation started.

干预措施: Benzydamine Hydrochloride 0.15% Oral Rinse (Drug)

Control Group

Placebo Comparator

Subjects who were allocated in control group would gargle with 15 ml of water before sedation started.

干预措施: Water (Drug)

结局指标

主要结局

Cumulative Propofol Consumption

时间窗: 90 minutes

About 1 mg/kg Propofol was initially administered to sedate the subjects. If the subject's RSS (Ramsay Sedation Scale) rose, 0.3 mg/kg was additionally given. The amount of propofol used, as in mg/kg, during the ERCP procedure was recorded.

Incidence of Sore Throat

时间窗: 4 hours

Sore throat incidence after ERCP procedure was recorded

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Adhrie Sugiarto

Medical Staff

Indonesia University

研究点 (1)

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