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临床试验/NCT01268189
NCT01268189已完成不适用

Evaluation of Oxygen Diffusion Dressing for Accelerating Healing of Donor Site and Other Wounds

United States Army Institute of Surgical Research2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2010年8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
20
试验地点
2
主要终点
Healing Time for Donor Site Wounds

研究概览

简要总结

This is a single-center, prospective, randomized, and controlled study to evaluate the effectiveness of OxyBand Dressing for the use as a dressing for autogenous skin donor sites compared to our current standard donor site dressing (Xeroform). Hypothesis is that the mean healing time for wounds treated with the OxyBand dressing will be less than the mean healing time for wounds treated with the Xeroform dressing.

详细描述

Patients who are scheduled for excision of burns or other injuries will have one of two donor sites covered with the OxyBand Dressing, and the other treated according to standard of care. OxyBand is an FDA (Food and Drug Administration) approved (K043063) wound dressing for delivery of oxygen into the wound. Two small clinical studies using OxyBand have been conducted on standardized laser burn wounds, demonstrating faster healing time compared to a placebo. No studies have compared this dressing to Xeroform dressing, the standard dressing used on donor sites in the USAISR.

研究设计

研究类型
Interventional
分配方式
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 must be at least 18 years of age; of either gender and in good general health.
  • Subject has sustained burn wounds of less than 30 percent of the total body surface area
  • Burn wounds do not involve the harvesting area
  • Subject has sustained burn wounds that, in the judgment of the attending surgeon, require excision and grafting of sufficient extent to justify two donor sites of equal and symmetrical size on non-dependent body surfaces areas
  • The scheduled excision and grafting procedure is the first such operation for the subject during this hospitalization
  • Subject agrees to participate in follow-up evaluations

排除标准

  • Critical illnesses such as those requiring ventilator support, or having a systemic infection or hemodynamic instability, defined as a mean arterial pressure less than 60 or requiring vasoactive medications to support blood pressure
  • Major acute or chronic medical illnesses that could affect wound healing (e.g. peripheral vascular disease, insulin dependent diabetes, blood clotting disorder)
  • Subjects receiving treatment with medications that inhibit or compromise wound healing. Examples include therapeutic anticoagulants, antiplatelet drugs, and systemic steroids such as warfarin, clopidogrel or prednisone. The use of anticoagulants does not include DVT (Deep Vein Thrombosis) prophylaxis. Subjects may use aspirin or lovenox
  • Cellulitis or other infection of the potential donor sites
  • Donor site has been previously harvested for grafting
  • Subjects with greater than 30% total body surface area burns
  • Pregnancy
  • Prisoners

结局指标

主要结局

Healing Time for Donor Site Wounds

时间窗: number of days to healing

Wounds are inspected on postoperative days 4, 8, and then every two days until the wound is deemed to be healed.

次要结局

  • Pain Perceived by Patient(Post-Operative Day 4)
  • Patient Will be Asked to Rate Pain 0-10/10 at the Study Site and the Control Site(Post-Operative Day 12)

研究者

发起方
United States Army Institute of Surgical Research
申办方类型
Fed
责任方
Sponsor

研究点 (2)

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