Comparison of Skinlink With Suture for ED Patients

Not Applicable

Completed

• Conditions: Wounds and Injuries; Lacerations
• Interventions: Other: Skinlink; Other: Nylon

• Registration Number: NCT02333877
• Lead Sponsor: Hallym University Kangnam Sacred Heart Hospital

Brief 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.

Detailed Description

Not available

Study Timeline

• Study Start: 2015-01
• Study First Submitted: 2015-01-04
• Study First Submitted QC: 2015-01-05
• Study First Posted: 2015-01-07
• Primary Completion: 2016-03
• Study Completion: 2016-04
• Status Verified: 2016-05
• Last Update Submitted: 2016-05-17
• Last Update Posted: 2016-05-18

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 49

Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Skinlink	Skinlink	applying Skinlink on simple laceration (length \< 5cm)
Nylon	Nylon	applying conventional suture using nylon on simple laceration (length \< 5cm)

Primary Outcome Measures

Name	Time	Method
Time required to complete suture	1year

Secondary Outcome Measures

Name	Time	Method
Dehiscence	1year
Infection rate	1year

Trial Locations

Locations (1)

Kangnam Sacred Heart Hospital; 🇰🇷 Seoul, Korea, Republic of