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临床试验/NCT00981604
NCT00981604已完成不适用

Single Incision Versus Laparoscopic Cholecystectomy

Children's Mercy Hospital Kansas City2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2009年8月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
60
试验地点
2
主要终点
Operative Time

研究概览

简要总结

Prospective randomized trial of single incision versus standard 4 port laparoscopic cholecystectomy. Hypothesis is that the operative time will be longer with single incision.

详细描述

This will be a prospective, randomized clinical trial involving patients who present to the hospital with an indication for cholecystectomy. We will offer enrollment to several institutions provided they receive institutional approval.

This will be a definitive trial design. Based on our operative times with SILS compared with our recent experience in standard laparoscopy, a sample size of 60 patients will give us a power of 0.8 with an α of 0.05.

After the procedure, both groups will be managed in the same manner per routine care. They will be discharged when tolerating a regular diet and their pain is well-controlled on oral pain medication.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
1 Year 至 18 Years(Child, Adult)
性别
All
接受健康志愿者

入选标准

  • Need for cholecystectomy

排除标准

  • Need for cholangiogram

结局指标

主要结局

Operative Time

时间窗: 1 day

次要结局

  • Operative complications(2 weeks)
  • length of hospitalization(1 week)
  • doses of analgesics(1 week)
  • hospital/operation charges(1 week)
  • surgeon perception of difficulty(1 day)
  • cosmetic scores(6 months)

研究者

发起方
Children's Mercy Hospital Kansas City
申办方类型
Other
责任方
Principal Investigator
主要研究者

Shawn St. Peter

MD

Children's Mercy Hospital Kansas City

研究点 (2)

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