跳至主要内容
临床试验/NCT03026543
NCT03026543已完成不适用

A Prospective, Blinded, Randomized Clinical Trial Investigating the Effect on Postoperative Pain and Nausea, When Performing a Ventilator-piloted PRM at the End of Laparoscopic Cholecystectomy

Region Östergötland2 个研究点 分布在 1 个国家目标入组 260 人开始时间: 2014年10月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
260
试验地点
2
主要终点
Change in postoperative pain assessed with a numeric rating scale

研究概览

简要总结

This prospective, blinded, randomized clinical trial investigates the effect on postoperative pain and nausea, when performing a ventilator-piloted PRM at the end of a laparoscopic cholecystectomy.

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, Care Provider, Investigator)

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

  • elective laparoscopic cholecystectomy
  • American Society of Anesthesiologists (ASA) physical status classification I-II (with the exception of body mass index over 35 kg/m2)
  • written consent

排除标准

  • conversion to open surgery
  • Clavien-Dindo grade ≥ II

结局指标

主要结局

Change in postoperative pain assessed with a numeric rating scale

时间窗: 4, 12, 24, 36 and 48 hours after surgery

A questionnaire with a numeric rating scale (NRS) is used to assess pain intensity at 4, 12, 24, 36 and 48 hours postoperatively.

次要结局

  • Change in postoperative nausea assessed with a Questionnaire(4, 12, 24, 36 and 48 hours after surgery)

研究者

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

Ebba Kihlstedt Pasquier

Principal Investigator

Region Östergötland

研究点 (2)

Loading locations...

相似试验