Trials / Completed
CompletedNCT02333877
Comparison of Skinlink With Suture for ED Patients
Comparison of Skinlink With Suture for ED Patients: a Randomized Controlled Trial
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 49 (actual)
- Sponsor
- Hallym University Kangnam Sacred Heart Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Skinlink | suture using Skinlink |
| OTHER | Nylon | conventional suture using nylon |
Timeline
- Start date
- 2015-01-01
- Primary completion
- 2016-03-01
- Completion
- 2016-04-01
- First posted
- 2015-01-07
- Last updated
- 2016-05-18
Locations
1 site across 1 country: South Korea
Source: ClinicalTrials.gov record NCT02333877. Inclusion in this directory is not an endorsement.