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临床试验/NCT02803164
NCT02803164已完成不适用

A Pilot Study to Evaluate the Efficacy of Vacuum-Assisted Dressings (V-AD) in the Management of Open Chest Wounds

Mayo Clinic2 个研究点 分布在 1 个国家目标入组 21 人开始时间: 2017年2月10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
Mayo Clinic
入组人数
21
试验地点
2
主要终点
Duration of Negative Pressure Wound Therapy (NWPT)

研究概览

简要总结

Vacuum-assisted dressings (V-AD) are effective in treating patients with open chest wounds (OCW) and will decrease the time-to-closure of such wounds when compared to a historical cohort of patients managed by traditional wound care management.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
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

  • Subject is scheduled to undergo surgical intervention(s) as part of the standard care for management of intra-thoracic infection.

排除标准

  • Patent bronchopleural fistulas. Severe respiratory failure requiring mechanical ventilation at the time of first consultation.
  • Proven or suspected malignancy in the wound. Coagulopathy due to medical or pharmacologic reasons. Dependency on anticoagulants or antiplatelet medication due to high risk for adverse events if these medications are stopped for a prolonged period of time.
  • Allergy to acrylic products.

结局指标

主要结局

Duration of Negative Pressure Wound Therapy (NWPT)

时间窗: 12 month follow up

The total number of days of receiving NWPT

次要结局

  • Length of Hospital Stay(12 months)
  • Wound Closure(12 months)

研究者

发起方
Mayo Clinic
申办方类型
Other
责任方
Principal Investigator
主要研究者

Mathew Thomas, M.D.

PI

Mayo Clinic

研究点 (2)

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