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临床试验/NCT02096224
NCT02096224已完成不适用

Comparison of the Effects of Sevoflurane and Desflurane on Prevention of Catheter-related Bladder Discomfort

Seoul National University Hospital1 个研究点 分布在 1 个国家目标入组 108 人开始时间: 2014年5月最近更新:
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
108
试验地点
1
主要终点
Catheter-related bladder discomfort

研究概览

简要总结

We want to evaluate the efficacy of the sevoflurane and desflurane for the prevention of catheter-related bladder discomfort.

详细描述

The mechanism of catheter-related bladder discomfort is thought to be related to the muscarinic receptor. The volatile anesthetics such as sevoflurane and desflurane are known to block the muscarinic receptor in different ways.

We want to evaluate the efficacy of the sevoflurane and desflurane for the prevention of catheter-related bladder discomfort.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients scheduled for transurethral bladder excision under general anesthesia
  • ASA I-III

排除标准

  • Bladder outflow obstruction
  • Overactive bladder
  • End-stage renal disease
  • Neurogenic bladder
  • Heart failure
  • Arrhythmia
  • Morbid obesity
  • Use of chronic analgesic medication
  • Hepatic disease
  • Pulmonary disease
  • Psychiatric disease

研究组 & 干预措施

Sevoflurane

Experimental

Sevoflurane will be administered as the maintenance agent of general anesthesia.

干预措施: Sevoflurane (Drug)

Desflurane

Active Comparator

Desflurane will be administered as the maintenance agent of general anesthesia.

干预措施: Desflurane (Drug)

结局指标

主要结局

Catheter-related bladder discomfort

时间窗: 24 hour postoperatively

Catheter-related bladder discomfort will be measured for 24 hour postoperatively (0:none, 1:mild, 2:moderate, 3:severe).

次要结局

  • Vomiting(0, 1, 6 and 24 hour postoperatively)
  • Dry mouth(0 houe after admission of operating room)
  • Catheter-related bladder discomfort(0, 1, 6 and 24 hour postoperatively)
  • Nausea(0, 1, 6 and 24 hour postoperatively)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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