N/A
N=12
Clinical Evaluation of the GLYDe Dressing for Post-surgical Incision Care
Post Surgical Incisions From Abdominoplasty Procedures
Bottom Line
View on ClinicalTrials.gov: NCT00766727 ↗Enrolled (actual)
12
Serious AEs
0.0%
Results posted
Dec 2020
Primary outcome: Primary: Scar Evaluation at End of Treatment Period Comparing Treated to Standard of Care (Control) — 18.64; 50.52 score on a scale
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- GLYDe Dressing (Device)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Neodyne Biosciences, Inc.
- Primary completion
- Nov 2009
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Scar Evaluation at End of Treatment Period Comparing Treated to Standard of Care (Control) |
18.64; 50.52 | — |
Summary
This study will evaluate a new dressing to be used for post-incision care for abdominoplasty patients. The hypothesis is that this dressing will minimize scar formation.
Eligibility Criteria
Inclusion Criteria
- subjects who have undergone an abdominoplasty 1 week prior to study participation
Exclusion Criteria
- subjects with a history of collagen vascular disease or scleroderma
- subjects with known adverse reactions to steri-strips, medical tapes or adhesives
Data sourced from ClinicalTrials.gov (NCT00766727). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.