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临床试验/NCT03716687
NCT03716687终止不适用

Prophylactic Negative Pressure Wound Therapy for High Risk Laparotomy Wounds. Randomized Prospective Clinical Trial.

St. Borbala Hospital2 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2018年11月1日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
发起方
入组人数
100
试验地点
2
主要终点
Surgical site infection

研究概览

简要总结

Negative pressure wound closure technique (NPWT) has been widely introduced in different clinical settings. Most of the studies report it as an effective and cost-effective method to treat complicated surgical wounds or even open abdomen.

NPWT as a prophylactic effort to prevent complications of high risk surgical wounds has recently been introduced, but the concept is still lacking clinical evidence in terms of clinical effectiveness and cost effectiveness.

In this randomized, multi centric study investigators aim to compare prophylactic negative pressure wound closure (ciNPWT) with traditional, dry wound dressing at high infection risk laparotomy wounds.

详细描述

The aim is to compare ciNPWT (closed incisional negative pressure wound dress) technique to the traditional, dry wound dressing technique at high infection risk laparotomy wounds.

Control arm will be treated "as usual": sterile gauze or high-absorbing surgical wound dress.

Experimental arm will be dressed with: one layer of silver-containing, impregnated mesh laxer (Atrauman® Ag - Hartmann) directly placed on the primary closed wound, one layer of alcohol-soaked foam (VivanoMed® White Foam - Hartmann) and sufficient-size sealant film (Hydrofilm® - Hartmann).

A negative pressure of -90 Hgmm will be administered in a continuous mode over 5 days postoperatively.

Surgical site infection and abdominal wall dehiscence rate will be assessed, as well as cost effectiveness will be calculated at both arms.

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
None

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • High risk laparotomy patients. SSI risk at least 3x higher than normal rate (6-8%)
  • Surgical wound type III or IV..

排除标准

  • Patients not giving informed consent.
  • Patients requiring open abdominal wound care.
  • Patients with abdominal wall malignancy,
  • Patients with peritoneal carcinomatosis,
  • Patients who are planned for second look laparotomy within 5 days,
  • Patients with less thank 3 month life expectancy.
  • Patients who are operated with existing wound infection

结局指标

主要结局

Surgical site infection

时间窗: 30 days

Surgical site infection requiring wound re-opening (suture removal) and open wound treatment. (Clavien-Dindo 2)

次要结局

  • Full thickness abdominal wall dehiscence, requiring re-operation(30 days)

研究者

发起方
St. Borbala Hospital
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Dr. Balázs Bánky PhD

Head of the Department of Surgery, St. Borbala Hospital

St. Borbala Hospital

研究点 (2)

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