跳至主要内容
临床试验/NCT00659542
NCT00659542已完成2 期

Randomized Study of Mesh Fixation With Absorbable Sutures or Glubran Tissue Sealant in Lichtenstein Hernioplasty

Kuopio University Hospital2 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2007年10月1日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
300
试验地点
2
主要终点
postoperative pain

研究概览

简要总结

The purpose of the study is to investigate whether chronic postoperative pain is less frequent and quality of life better when inguinal mesh is fixed by using tissue glue compared to conventional sutures in inguinal hernioplasty.

详细描述

Repair of inguinal hernia in one of the most frequently performed surgical operation in western world. The technique of choice is currently to support inguinal tissues by using polypropylene mesh. Chronic postoperative pain and discomfort occur in 25-30% of patients after inguinal hernioplasty. Pain might be related to mesh fixation by sutures. This randomized study investigates whether mesh fixation by tissue glue (cyanoacrylate) is better than sutures. The patients are followed 1 year postoperatively. Pain, quality of life, operative parameters (time, cost) and recurrences are reported.

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
Single (Participant)

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

  • inguinal hernia
  • adult patient

排除标准

  • patient not willing
  • multiple recurrences
  • inguinal pain without evidence of hernia
  • femoral hernia
  • large scrotal hernia

结局指标

主要结局

postoperative pain

时间窗: 1 year

次要结局

  • hernia recurrence, quality of life(1 year)

研究者

发起方
Kuopio University Hospital
申办方类型
Other

研究点 (2)

Loading locations...

相似试验

Glubran Mesh Fixation in Lichtenstein Hernioplasty | 临床试验