Comparison of Skinlink With Suture for ED Patients
Not Applicable
Completed
- Conditions
- Wounds and InjuriesLacerations
- 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
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
- Primary Outcome Measures
Name Time Method Time required to complete suture 1year
- Secondary Outcome Measures
Name Time Method Dehiscence 1year Infection rate 1year
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie the faster wound healing observed with Leukosan Skinlink in ED patients compared to nylon sutures?
How does the efficacy of Leukosan Skinlink compare to standard-of-care sutures for simple lacerations in emergency department settings?
Are there specific biomarkers that can predict optimal patient selection for Leukosan Skinlink versus traditional suture techniques in wound repair?
What are the potential adverse events associated with Leukosan Skinlink in ED wound closure and how do they compare to nylon sutures?
What alternative wound closure technologies or compounds are being developed as competitors to Leukosan Skinlink for emergency laceration repair?
Trial Locations
- Locations (1)
Kangnam Sacred Heart Hospital
🇰🇷Seoul, Korea, Republic of
Kangnam Sacred Heart Hospital🇰🇷Seoul, Korea, Republic of