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临床试验/NCT04997174
NCT04997174Unknown不适用

Comparison of Postoperative Pain Management in Patients Undergoing Laparoscopic Colorectal Surgery Under Enhanced Recovery After Surgery (ERAS) Program, Laparoscopic Colorectal Surgery Without ERAS and Open Colorectal Surgery

Prince of Songkla University1 个研究点 分布在 1 个国家目标入组 162 人开始时间: 2021年10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
入组人数
162
试验地点
1
主要终点
Pain intensity

研究概览

简要总结

This is a retrospective study to compare postoperative pain intensity in patients going laparoscopic colorectal surgery with Enhanced Recovery after Surgery (ERAS), without ERAS and open colorectal surgery.

详细描述

This study is a matched case-control study. Control patients will be matched to ERAS cases in a 1:1:1 ratio (laparoscopic surgery with ERAS protocol : laparoscopic surgery without ERAS protocol : open surgery).

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Retrospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Patients undergoing colorectal surgery under ERAS program and those with the same sort of laparoscopic surgery without ERAS program as well as those with open colorectal surgery with complete required recorded data.

排除标准

  • Patients with incomplete required data on record.
  • Those with any major intraoperative or postoperative complications.

研究组 & 干预措施

ERAS

Patients undergoing laparoscopic colorectal surgery with ERAS

干预措施: Celecoxib (Drug)

结局指标

主要结局

Pain intensity

时间窗: Until discharge (5-7 days)

Pain score (Verbal Numerical Rating Scale: VNRS) after surgery, VNRS consists of 0-10, where 0 means no pain and 10 means worst pain imaginable

次要结局

  • Opioid(Until discharge (5-7 days))

研究者

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

Sasikaan Nimmaanrat

Associate Professor

Prince of Songkla University

研究点 (1)

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