NL-OMON33251已完成不适用
Randomised controled trial comparing the effect of a new self-gripping semi-resorbable Parietene Progrip mesh and the sutured Polypropylene mesh on the incidence of chronic inguinodynia in Lichtenstein hernioplasty. - Inguinodynia after Lichtenstein: Polypropylene versus Parietene Progrip
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 400
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
- 年龄范围
- 18 至 99（—）
入选标准
- •1. Capacitated male person, age 18 years or older
- •2. Unilateral inguinal hernia
排除标准
- •1. Concurrent femoral hernia
- •2. Incarcerated inguinal hernia
- •3. ASA 4 or more
- •4. Adequate follow up impossible because of mental retardation, dementia, foreign language speaker.
研究者
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