Trials / Completed
CompletedNCT02223689
Evaluation of Skin Affix in the Emergency Room
Evaluation of SkinAffix as a Topical Emergency Room Department Skin Incision Adhesive
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 35 (actual)
- Sponsor
- Medline Industries · Industry
- Sex
- All
- Age
- 5 Years
- Healthy volunteers
- Not accepted
Summary
Effectiveness of a surgical adhesive on wounds found in Emergency Medicine.
Detailed description
Subjects were approached for recruitment in the ED when discussing closure options by the physician. Only subjects deemed appropriate for skin glue closures by their treating physician were approached.Subjects were followed at 48 hours post-procedure, 5-10 days, and at 14 days following the ED visit.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Skin Affix |
Timeline
- Start date
- 2014-07-01
- Primary completion
- 2016-03-01
- Completion
- 2016-09-01
- First posted
- 2014-08-22
- Last updated
- 2019-08-07
- Results posted
- 2019-07-11
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT02223689. Inclusion in this directory is not an endorsement.