跳至主要内容
临床试验/ISRCTN31866667
ISRCTN31866667已完成不适用

Inguinal hernia management: operation or observation? A randomised controlled multicentre trial

Erasmus Medical Centre (Netherlands)0 个研究点目标入组 800 人开始时间: 2005年12月20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
800

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

性别
Male

入选标准

  • 1. Unilateral inguinal hernia
  • 3. Medial or lateral inguinal hernia
  • 4. Aged greater than or equal to 50 years
  • 5. Description I or II of pain or discomfort interfering with daily activity
  • 6. Primary or recurrent inguinal hernia
  • 7. Informed consent (addendum V)

排除标准

  • 1. Gender: female
  • 2. Bilateral inguinal hernia
  • 3. Femoral hernia
  • 4. Description III or IV of pain or discomfort interfering with daily activity
  • 5. Acute hernia complication (bowel obstruction, incarceration, strangulation, peritonitis or perforation)
  • 6. Patient classified as American Society of Anaesthesiologist Class 4
  • 7. Scrotal hernia (cannot be corrected laparoscopically)
  • 8. Patient is unable to speak Dutch
  • 9. Physical activity: patient travels regularly during which professional medical help is not always accessible
  • 10. Inguinal hernia not apparent during ultrasonography

研究者

发起方
Erasmus Medical Centre (Netherlands)

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