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临床试验/NCT02255877
NCT02255877撤回4 期

A Prospective, Non Blinded, Randomized Controlled Post Market Study Designed to Compare the Use of the Zip Surgical Skin Closure Device vs. Conventional Steel Staples for Skin Closure in Subjects Who Undergo a bi Lateral Knee Arthroplasty

ZipLine Medical Inc.2 个研究点 分布在 1 个国家开始时间: 2014年9月最近更新:
适应症

试验速览

阶段
4 期
状态
撤回
试验地点
2
主要终点
Effectiveness Outcome - Wound Healing

研究概览

简要总结

Study designed to evaluate the Zip Surgical Skin Closure device versus conventional steel staple placement when utilized for surgical wound closure after bi lateral unicompartmental or bi later total knee replacement.

详细描述

This is a randomized, within patient control study aiming to enroll up to 25 subjects requiring bi lateral knee arthroplasty (unicompartmental or toal) at a single study center. Subjects will be followed for up for 6 weeks post surgery to evaluate wound healing and overall satisfaction of closure methods.

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

  • Patients requiring epidermal closure after bi lateral total or partial (unicompartmental) knee arthroplasty;
  • Patients willing to be evaluated at discharge and 6-weeks post op.

排除标准

  • Known bleeding disorder not caused by medication
  • Known personal or family history of keloid formation or scar hypertrophy
  • Known allergy or hypersensitivity to non-latex skin adhesives
  • Atrophic skin deemed clinically prone to blistering
  • Any skin disorder affecting wound healing
  • Any other condition that in the opinion of the investigator would make a particular patient unsuitable for this study

结局指标

主要结局

Effectiveness Outcome - Wound Healing

时间窗: 6 weeks post surgery

Wound healing as judged by the Cosmetic Visual Analogue Scale - Photos taken at 6 weeks post surgery will be judged by panel of Plastic Surgeons blinded to the treatment assignments.

次要结局

  • Patient Satisfaction of Scars(At 6 week Follow up (exit) visit)
  • Patient Pain(Throughout 6 week study period (Discharge, 2 week follow up and 6 week follow up (exit) visits.))
  • Surgeon Satisfaction with the Closure Method(At Discharge, 1-3 days post surgery)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (2)

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