跳至主要内容
临床试验/NCT03159130
NCT03159130撤回不适用

OnQ Pain Pump Effectiveness in Post Operative Pain Control in Bariatric Patients

William Beaumont Army Medical Center1 个研究点 分布在 1 个国家开始时间: 2012年6月最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
试验地点
1
主要终点
Narcotic use

研究概览

简要总结

This study will assess the efficacy of OnQ pain catheters in pain reduction in the bariatric surgical population and seeks to identify if a quantifiable improved post-operative course occurs in patients receiving a catheter filled with local anesthetic versus that achieved by patients who receive a catheter filled with injectable saline.

详细描述

This study will assess the efficacy of OnQ pain catheters in pain reduction in the bariatric surgical population. Approximately 12 to 15 weight reduction surgeries are performed at William Beaumont Army Medical Center each month. It is the current practice that each patient receiving the laparoscopic gastric sleeve or laparoscopic Roux-en-Y gastric bypass receive an OnQ pain catheter during the surgery to reduce post-operative pain. There have been limited studies to quantify the efficacy of these devices. This study will seek to identify if a quantifiable improved post-operative course occurs in patients receiving a catheter filled with local anesthetic versus that achieved by patients who receive a catheter filled with injectable saline.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

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

  • Meets criteria for Bariatric surgery
  • Consents to be in protocol
  • No local anesthetic allergy
  • Will be having sleeve gastrectomy
  • Doesn't have extensive scarring of abdominal wall that would prevent placement of OnQ catheter

排除标准

  • declines to participate

结局指标

主要结局

Narcotic use

时间窗: from admission to recovery room until discharge from the hospital (3-5 days)

immediate post-operative narcotic use per patient

次要结局

未报告次要终点

研究者

申办方类型
Fed
责任方
Sponsor

研究点 (1)

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