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Comparison of Skinlink With Suture for ED Patients — Skinlink  

Wounds and Injuries Clinical Trial

Official title:
Comparison of Skinlink With Suture for ED Patients: a Randomized Controlled Trial

Clinical Trial Summary

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.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02333877
Study type Interventional
Source Hallym University Kangnam Sacred Heart Hospital
Contact
Status Completed
Phase N/A
Start date January 2015
Completion date April 2016
View Details
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