跳至主要内容
临床试验/NCT02559453
NCT02559453Unknown不适用

A Randomized Trial Comparing the Outcomes for 2 Operations Versus ≥ 3 Operations in Infected Wounds Requiring Hospitalization

Georgetown University0 个研究点目标入组 250 人开始时间: 2015年9月最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
250
主要终点
Number of post-hospital discharge complications between subjects who received 2 versus 3 or more debridement operations prior to closure.

研究概览

简要总结

We have designed this study to determine whether performing two, compared with ≥3 operations has an effect on key clinical outcomes after discharge from the hospital of an infected wound that requires admission. Each arm of this study represents the two commonly practiced standard of care treatment plans for patients presenting with infected wounds. It is currently unknown which SoC option provides the best patient outcome.

详细描述

There is a lack of consensus about whether or not a patient with an infected wound requires more than 2 surgical procedures. For patients admitted for an infected wound this study will investigate whether 2, compared with ≥3, operative interventions results in better outcomes. All patients admitted for an infected wound will be assessed for eligibility in the study. If eligible, subjects will be randomized into Cohort A (2 operative visits) or Cohort B (≥3 operative visits). Subjects will then be followed during the hospitalization as well as 180 days post discharge.

A total of 250 subjects will be enrolled into this study. Two operations (n=125) will be compared with ≥3 operations (n=125) during the hospitalization. We will compare the following factors between the two treatment groups: length of hospital stay; readmission post-discharge; quality of life; proportion of wounds closed or covered with a graft; culture results; host factors; environmental factors post-hospital discharge; and, financial charges related to admission and readmission. We expect full enrollment to take 3 years in duration.

Debridement of the wound will be performed in the customary manner per SOC in the operating room. Prior to the start of the study, the surgeons performing the operations will be required to view a video that demonstrates the standardized debridement technique that will be utilized. The following is the standardized technique depicted in the video:

All wound surfaces will be painted with dye prior to debridement. Debridement involves the use of a scalpel, scissors, curette, rongeur, or hydro-surgery. A 2-3 millimeter skin edge around the perimeter of the wound will also be resected. All infected/nonviable tissue will be removed and all tissues with dye will be surgically removed. This includes decompression of any purulent material and excision of any indurated tissue (until tissue pliability is established). Nonviable tissue includes necrotic and fibrous tissue. Debridement will be performed until the there is bleeding on the wound base and perimeter.

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
Single (Care Provider)

入排标准

年龄范围
18 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Infected wound requiring hospital admission
  • Infected wound requiring an operative intervention
  • Wound can be located anywhere on the body
  • Patient able and willing to comply with all study requirements

排除标准

  • Planned free tissue flap for soft tissue reconstruction
  • Wound located over exposed joint implant
  • Wound located over exposed hardware
  • Disease or treatment causing substantial immunosuppression
  • History of collagen vascular disease
  • Transplant recipient
  • Venous stasis ulcer
  • Radiation-induced ulcer
  • Contraindication for use of negative pressure wound therapy with instillation of normal saline
  • Unable or unwilling to comply with study requirements

研究组 & 干预措施

2 operations

Active Comparator

Subjects in this arm will receive a maximum of two surgical debridements of their wound.

干预措施: Debridement (Procedure)

3 or more operations

Active Comparator

Subjects in this arm will receive three or more surgical debridements of their wound.

干预措施: Debridement (Procedure)

结局指标

主要结局

Number of post-hospital discharge complications between subjects who received 2 versus 3 or more debridement operations prior to closure.

时间窗: 180 Days

次要结局

未报告次要终点

研究者

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

Christopher Attinger, M.D.

Director of the Center for Wound Healing

Georgetown University

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