Clinical Trials Directory

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

TypeNameDescription
DEVICESurgisealsurgical 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.