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Comparison of Skinlink With Suture for ED Patients

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02333877
Acronym
Skinlink
Enrollment
49
Registered
2015-01-07
Start date
2015-01-31
Completion date
2016-04-30
Last updated
2016-05-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lacerations, Wounds and Injuries

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.

Interventions

OTHERSkinlink

suture using Skinlink

OTHERNylon

conventional suture using nylon

Sponsors

Hallym University Kangnam Sacred Heart Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

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

Design outcomes

Primary

MeasureTime frame
Time required to complete suture1year

Secondary

MeasureTime frame
Dehiscence1year
Infection rate1year

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026