Trials / Completed
CompletedNCT01514396
Skin Incision Adhesive in Pediatrics
Evaluation of Surgiseal as a Topical Emergency Department Skin Incision Adhesive in Pediatrics A Case Series
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 8 (actual)
- Sponsor
- Medline Industries · Industry
- Sex
- All
- Age
- 5 Years – 18 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to evaluate the effectiveness of on-label use of Surgiseal™ Tissue Adhesive, a cyanoacrylate-based Surgical Topical Skin Tissue Adhesive in wound closure of the topical skin in children presenting in the Emergency Department (ED).
Detailed description
Subjects had SurgiSeal™ applied to their topical skin incisions in the ED. Subjects' wounds were evaluated for bleeding and closure of the incision/wound before patient discharge and 48 hours after the procedure. Further follow up wound closure evaluations were conducted via telephone interview at 5-10 days and 14 days after the ED visit.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Surgiseal | surgical glue |
Timeline
- Start date
- 2013-02-01
- Primary completion
- 2014-08-01
- Completion
- 2014-08-01
- First posted
- 2012-01-23
- Last updated
- 2018-12-04
- Results posted
- 2018-12-04
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01514396. Inclusion in this directory is not an endorsement.