跳至主要内容
临床试验/NCT01002287
NCT01002287终止不适用

An Evaluation of the SprayShield Adhesion Barrier System in Reducing Post-Operative Adhesion in Abdominal Surgery

Integra LifeSciences Corporation2 个研究点 分布在 1 个国家目标入组 11 人开始时间: 2009年10月最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
11
试验地点
2
主要终点
The Incidence of Adhesions, Defined as the Proportion of Subjects Presenting at the Follow-up Surgery (10-12 Weeks) With One or More Adhesions to the Midline Incision, Regardless of Extent and/or Severity.

研究概览

简要总结

This will be a prospective, multi-center, randomized, single blind study to collect and evaluate post-market clinical data on the SprayShield Adhesion Barrier System as an adjuvant to good surgical technique for the reduction of postoperative adhesion formation following major open abdominal surgery.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Participant)

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

  • Diagnosis of ulcerative colitis or familial polyposis and require two-stage surgery for treatment of either of these disorders will be eligible

排除标准

  • 未提供

结局指标

主要结局

The Incidence of Adhesions, Defined as the Proportion of Subjects Presenting at the Follow-up Surgery (10-12 Weeks) With One or More Adhesions to the Midline Incision, Regardless of Extent and/or Severity.

时间窗: 10-12 Weeks post Initial Surgery for J-Pouch

次要结局

  • Severity of Adhesions(Average 10-12 weeks post surgery)
  • Adhesion Involvement Along the Midline Incision (Percentage)(average 10-12 weeks post surgery)
  • Mobilization Time(average 10-12 weeks post surgery)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

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