NCT02333877已完成不适用
Comparison of Skinlink With Suture for ED Patients: a Randomized Controlled Trial
Hallym University Kangnam Sacred Heart Hospital1 个研究点 分布在 1 个国家目标入组 49 人开始时间: 2015年1月1日最近更新:
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 49
- 试验地点
- 1
- 主要终点
- Time required to complete suture
研究概览
简要总结
The purpose of this study is to determine whether suture using the Device of "Leukosan Skinlink" is more faster and safer than that of "nylon" in the treatment of simple wound for ED patients.
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
- None
入排标准
- 年龄范围
- 18 Years 至 75 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •The inclusion criteria were age 18-75 years,presence of a partial thickness laceration, generally good health without systemic abnormalities,agreement to return for a 14-day follow-up, and written informed consent. The
排除标准
- •were previous diagnosis of diabetes mellitus, peripheral vascular disease, or bleeding disorders; history of keloid formation or scar hypertrophy; and allergy to cyanoacrylate compounds or formaldehyde
研究组 & 干预措施
Skinlink
Experimental
applying Skinlink on simple laceration (length < 5cm)
干预措施: Skinlink (Other)
Nylon
Other
applying conventional suture using nylon on simple laceration (length < 5cm)
干预措施: Nylon (Other)
结局指标
主要结局
Time required to complete suture
时间窗: 1year
次要结局
- Dehiscence(1year)
- Infection rate(1year)
研究者
Kim Hyeongtae
Residency
Hallym University Kangnam Sacred Heart Hospital
研究点 (1)
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