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临床试验/NCT01974882
NCT01974882已完成不适用

Minimizing Post-surgical Pain and Narcotic Administration Through Cryotherapy

Viraj Master4 个研究点 分布在 1 个国家目标入组 55 人开始时间: 2008年5月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
55
试验地点
4
主要终点
Change in postoperative pain score

研究概览

简要总结

Postoperative pain is an unavoidable consequence of open abdominal surgery. Although cryotherapy, the application of ice to a surgical wound site, has been shown to be effective in reducing postoperative pain in orthopedic, gynecologic, and hernia operations, it has not been assessed in patients who undergo major open abdominal operations. We hypothesized that patients who receive cryotherapy would report lower pain scores as a primary outcome measure. This would result in less narcotic analgesia usage, and shorter hospital stays as secondary outcome measures.

详细描述

Objectives:

This study will attempt to assess the impact of cryotherapy on post-surgical inflammation and narcotic use. End-points for the study will be patient use of narcotics and pain level, regularly measured by nursing staff.

Patient Selection:

This study will accept all consecutive consenting patients who visit the Grady Hospital and Emory University urology clinics who require abdominal surgery.The study will require 55 patients, based on prior power calculations.

Registration/Randomization:

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
None

入排标准

年龄范围
18 Years 至 89 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Any open transperitoneal abdominal surgery with a midline incision

排除标准

  • Additional surgeries required

结局指标

主要结局

Change in postoperative pain score

时间窗: Participants will be followed for the duration of hospital stay, an average of 7 days

Throughout the hospital stay nurses will assess patients pain levels. Patients will complete a visual analog score one hour postoperatively and then at 8am and 4 pm each day.

次要结局

  • Narcotic use(Participants will be followed for the duration of hospital stay, an average of 7 days)

研究者

发起方
Viraj Master
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Viraj Master

Director of Clinical Research Unit

Emory University

研究点 (4)

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