跳至主要内容
临床试验/NCT04916067
NCT04916067终止不适用

Stoma Closure and Reinforcement (SCAR)-II Trial: A Single Center Pilot Study of the Safety of a Mesh Reinforcement of Ileostomy Closure to Prevent Hernia Formation in Inflammatory Bowel Disease Patients

Dartmouth-Hitchcock Medical Center2 个研究点 分布在 1 个国家目标入组 7 人开始时间: 2021年12月1日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
7
试验地点
2
主要终点
Incidence of wound occurrences

研究概览

简要总结

Hernia formation at sites of ostomy closure is a common complication. The investigator believes that using evidence based hernia repair techniques as a preventive measure during closure of ostomies will reduce the incidence of hernia formation. In this trial, the investigator will pilot a novel technique of monofilament bioresorbable mesh reinforcement of the abdominal wall defects that remain after closure of an ileostomy to evaluate for safety and begin to evaluate the effectiveness compared to standard techniques.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

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

  • Age > 18years.
  • Patient is undergoing closure of loop ileostomy.
  • Patient has a diagnosis of Inflammatory bowel disease treated with resection and diverting loop ileostomy.
  • Patient has been evaluated by a qualified surgeon and found to be a suitable candidate for surgery.

排除标准

  • Pre-existing systemic infection at the time of ileostomy takedown
  • Cirrhosis, chronic renal failure requiring dialysis, or collagen disorder
  • Previous abdominal hernia repair with mesh placement
  • Concurrent surgical procedures in addition to closure of diverting loop ileostomy
  • Ileostomy closure not completed through the previous stoma site (i.e. those requiring exploratory laparotomy for closure)

结局指标

主要结局

Incidence of wound occurrences

时间窗: 30 days

Incidence of wound occurrences (defined as superficial surgical site infection \[s-SSI\], deep surgical site infection \[d-SSI\], organ space surgical site infection \[O-SSI\], dehiscence, and seroma formation) at 30 days, with particular attention to wound occurrences requiring procedural intervention, including but not limited to, operative debridement, radiographically guided drain placement, or excision of the mesh will be assessed.

次要结局

  • Quality of Life after mesh implantation(30 days, 6 months)
  • Bowel Function after mesh implantation(30 days, 6 months)
  • Incidence of hernia formation(30 days, 6 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Matthew Z. Wilson

Assistant Professor of Surgery

Dartmouth-Hitchcock Medical Center

研究点 (2)

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