Trials / Completed
CompletedNCT03312166
Compressive Device to Prevent Keloïd Scars Recurrence [SCARWARS]
First Study Evaluating Efficiency and Safety of a Compressive Device to Prevent Keloid Scars Recurrence After Surgery
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 31 (actual)
- Sponsor
- Centre Hospitalier Universitaire de Besancon · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
SCARWARS study deals with the first on-human evaluation of a compressive device dedicated to the prevention of keloïd scars recurrence after surgery. The tested device is made with clinical grade silicon. SCARWARS is a monocentric study. 27 patients will be include and follow during one year. The primary outcome of this study is the number of keloid recurrence after treatment.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Compression device | interventions on patient are : * surgical excision of ear lobe keloid * application of compression device on sutured skin |
Timeline
- Start date
- 2017-10-03
- Primary completion
- 2023-12-14
- Completion
- 2023-12-14
- First posted
- 2017-10-17
- Last updated
- 2024-09-19
Locations
1 site across 1 country: France
Source: ClinicalTrials.gov record NCT03312166. Inclusion in this directory is not an endorsement.