Mesh Fixation With a Synthetic Glue in Primary Inguinal Hernia Repair
试验速览
- 阶段
- 不适用
- 入组人数
- 150
- 试验地点
- 1
- 主要终点
- Postoperative pain (Evaluation will be conducted through scale and a questionnaire )
研究概览
简要总结
Prospective observational study with mesh fixation using FDA approved synthetic glue,glubran 2 and standard mesh fixation with stiches in primary inguinal hernia repair surgery. The investigators aim is to recruit 150 patients for the study.
The outcomes The investigators would like to determine are : postoperative pain,recurrences and complication rates such as seromas.
详细描述
Prospective observational study with mesh fixation using FDA approved synthetic glue,glubran 2 and standard mesh fixation with stiches in primary inguinal hernia repair surgery. The investigators aim is to recruit 150 patients for the study.
The outcomes The investigators would like to determine are : postoperative pain,recurrences and complication rates such as seromas.
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 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Primary Inguinal hernia
排除标准
- •Recurrent hernia
- •Large inguinoscrotal hernias
- •Bilateral inguinal hernias
结局指标
主要结局
Postoperative pain (Evaluation will be conducted through scale and a questionnaire )
时间窗: 2 years
次要结局
- Hernia recurrence (Evaluation will be conducted through a questionnaire and physical examination )(2 years)
- Postoperative complications (Evaluation will be conducted through a questionnaire and physical examination )(2 years)