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OpenTrials
Completed

NCT Number: NCT02333877

Comparison of Skinlink With Suture for ED Patients

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.

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Key information

Conditions

Wounds and Injuries Lacerations

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Kangnam Sacred Heart Hospital

Seoul, ASI|KR|KS013|SEOUL, South Korea

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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 exclusion criteria 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

Treatment and study plan

Skinlink

Other

suture using Skinlink

Nylon

Other

conventional suture using nylon

Primary outcomes

  1. Time required to complete suture

    Time frame: 1year

Secondary outcomes

  1. Dehiscence

    Time frame: 1year

  2. Infection rate

    Time frame: 1year

Sponsors and collaborators

Lead sponsor

Hallym University Kangnam Sacred Heart Hospital

Other

Registry information

Official study title

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

Acronym: Skinlink

Important dates

Study start
2015
Primary completion
2016
Study completion
2016
First posted
Jan 7, 2015
Registry last updated
May 18, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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