跳至主要内容
临床试验/NCT00766727
NCT00766727已完成不适用

Clinical Evaluation of the GLYDe Dressing for Post-surgical Incision Care

Neodyne Biosciences, Inc.2 个研究点 分布在 1 个国家目标入组 12 人开始时间: 2008年10月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
12
试验地点
2
主要终点
Scar Evaluation at End of Treatment Period Comparing Treated to Standard of Care (Control)

研究概览

简要总结

This study will evaluate a new dressing to be used for post-incision care for abdominoplasty patients. The hypothesis is that this dressing will minimize scar formation.

详细描述

This study will evaluate a new dressing in up to 30 patients who have undergone an abdominoplasty procedure. They will wear the dressing through 8 weeks post surgery and the scar will be evaluated at 3 months post surgery.

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 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • subjects who have undergone an abdominoplasty 1 week prior to study participation

排除标准

  • subjects with a history of collagen vascular disease or scleroderma
  • subjects with known adverse reactions to steri-strips, medical tapes or adhesives

结局指标

主要结局

Scar Evaluation at End of Treatment Period Comparing Treated to Standard of Care (Control)

时间窗: through 12 months

Professional photographs were taken 12 months postsurgery and evaluated by lay and professional panels. A 100 point Visual Analog Scale (VAS), ranging from a score of 0 for a better outcome to a score of 100 for worse outcome, will be used to assess both the Treated and Control scars at the same timepoint.

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

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