ACTRN12621000643875终止未知
aparoscopic Articulated Continuous Suture vs tacks in patients with a ventral hernia repair, a randomised controlled trial to assess pain and mobility post-operatively.
适应症
试验速览
- 阶段
- 未知
- 状态
- 终止
- 入组人数
- 11
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomised controlled trial
- 主要目的
- Treatment
- 盲法
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •All patients undergoing an elective laparoscopic repair of ventral hernia will be included provided they meet the following criteria:
- •Age 18 years or over
- •Provide written consent to participate in the study
- •Hernia defect size of 2-10cm as measured intra-operatively with insufflation pressure of 12mmHg
- •Hernia considered suitable for laparoscopic repair with either suture or tack fixation of mesh by operating surgeon
- •Proposed permanent coated mesh determined to be suitable for intra-peritoneal placement by the treating surgeon
排除标准
- •Patients will be excluded from the trial if they meet the following exclusion criteria:
- •Recurrent hernia with previous intraperitoneal mesh
- •Known allergic reaction to bupivacaine or ropivacaine
- •Large (>10cms) hernias not suitable for laparoscopic repair
- •Umbilical defects most appropriate for open primary suture repair
- •Incarcerated, strangulated or obstructed hernias booked as emergency cases.
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