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临床试验/NCT06068517
NCT06068517尚未招募不适用

Closed Incision Negative Pressure Wound Therapy for the Prevention of Surgical Site Infections in Abdominal Surgery - A Multicenter Randomized Controlled Trial

Insel Gruppe AG, University Hospital Bern2 个研究点 分布在 1 个国家目标入组 654 人开始时间: 2026年3月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
654
试验地点
2
主要终点
Composite incidence of superficial and deep surgical site infections

研究概览

简要总结

Surgical site infections (SSI) are a frequent complication in abdominal surgery. SSI lead to worse outcomes for the affected patients and significantly higher healthcare costs. Closed incision negative pressure wound therapy (ciNPWT) consists of a non-invasive, vacuum-assisted system that applies negative pressure to closed surgical incisions. It is currently unclear, if ciNPWT reduces SSI in patients undergoing abdominal surgery. This trial will investigate the effect of ciNPWT on SSI in abdominal surgery.

详细描述

Background:

Surgical site infections (SSI) are a frequent complication after abdominal surgery and are associated with increased morbidity and mortality, longer hospital stay, and significantly increased healthcare costs. Closed incision negative pressure wound therapy (ciNPWT) is a non-invasive, vacuum-assisted system that applies negative pressure to closed surgical incisions. Recent meta-analyses suggest that ciNPWT reduces the risk of SSI in abdominal surgery. However, based on the available randomized controlled trials (RCT), the evidence for the effect of ciNPWT on SSI in abdominal surgery is insufficient.

Rationale:

Considering the frequent occurrence of SSI in abdominal surgery, associated worse outcomes, and insufficient evidence, an adequately powered, robust RCT investigating the effect of ciNPWT on SSI in elective and emergency abdominal surgery is warranted. Provided that ciNPWT significantly reduces the incidence of SSI, this adjunct to surgical therapy has the potential to fundamentally improve patient outcomes in abdominal surgery.

Aim of the trial:

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
19 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Elective or emergency laparotomy, or laparoscopy converted to laparotomy, including surgery for complications after elective operations
  • Incision length ≥ 10 cm
  • Centers for Disease Control and Prevention (CDC) wound class 1 and 2 (clean, clean-contaminated)
  • Abdominal closure with or without mesh implantation
  • Primary abdominal closure or closure after open abdomen treatment
  • Age over 18 years
  • Written informed consent

排除标准

  • Age ≤ 18 years
  • CDC wound class 4 (dirty/infected wound)
  • Organ transplantation
  • Sensitivity or allergy to silver

结局指标

主要结局

Composite incidence of superficial and deep surgical site infections

时间窗: 30 (+/- 7) days

Number of participants with a superficial or deep surgical site infections at 30 (+/- 7) days postoperatively.

次要结局

  • Duration of closed incision negative pressure wound therapy(7 days)
  • Overall surgical site infections (superficial, deep, and organ space)(30 (+/- 7) days)
  • Postoperative hospital length of stay(Usually between 1 and 14 days)
  • Superficial, deep, and organ space surgical site infections as separate outcomes(30 (+/- 7) days)
  • Other wound complications (wound dehiscence, seroma, hematoma)(30 (+/- 7) days)
  • Number of outpatient visits(30 days)
  • Costs for inpatient treatment(Usually between 1 and 14 days)
  • In-hospital mortality(Usually between 1 and 14 days)
  • Postoperative health-related quality of life (SF-36 Health Survey)(30 (+/- 7) days)
  • 30-day mortality(30 days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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