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临床试验/NCT01889394
NCT01889394已完成不适用

Primary Wound Closure Using a Limberg Flap Versus Secondary Wound Healing Following Pilonidal Sinus Excision: Short-term Results of a Randomized Controlled Multicenter Trial

Kantonsspital Liestal5 个研究点 分布在 1 个国家目标入组 102 人开始时间: 2006年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
102
试验地点
5
主要终点
Inability to work

研究概览

简要总结

To compare primary wound closure using a limberg flap with secondary (p.s.) wound healing following excision of a pilonidal sinus.

详细描述

Patients who gave their informed consent who had excision of pilonidal sinus were randomly assigned to group A (primary wound closure with a Limberg flap) or to group B (open wound and p.s.wound healing).

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
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

  • indication for excision of pilonidal sinus given

排除标准

  • limberg flap not possible for surgical reasons

结局指标

主要结局

Inability to work

时间窗: 1 year

change for capacity for work at one year post-OP

次要结局

  • Pain perioperatively and after 3 weeks(0 and 3 weeks)
  • Patient satisfaction after 3 weeks & 1year(3 weeks and 1 year)
  • Complication rate after 3 weeks(3 weeks)
  • Recurrence rate after 1 year(1 year)

研究者

发起方
Kantonsspital Liestal
申办方类型
Other
责任方
Sponsor

研究点 (5)

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