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Zip® Surgical Skin Closure Device vs. Staples for Skin Closure in Subjects Having Undergone Bilateral Knee Arthroplasty

Wound Healing Clinical Trial

Official title:
A Prospective, Randomized Controlled Post-market Study to Compare the Use of the Zip® Surgical Skin Closure Device Versus Conventional Staples for Skin Closure in Subjects Having Undergone Bilateral Knee Arthroplasty

Clinical Trial Summary

Study designed to compare the Zip Surgical Skin Closure device vs. conventional staples for wound closure following bi lateral knee replacement surgery.

Clinical Trial Description

Prospective, randomized, within patient control study comparing the use of Zip Surgical Skin Closure device versus conventional staple placement when utilized for surgical wound closure after bi lateral unicompartmental or bi lateral total knee replacement. A total of up to 25 patients will be enrolled and followed for up to 8 weeks post surgery to evaluate wound healing and overall satisfaction of closure method. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02460172
Study type Interventional
Source ZipLine Medical Inc.
Contact
Status Completed
Phase N/A
Start date May 2015
Completion date February 15, 2017
View Details
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