Viewing Study NCT03312166


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Study NCT ID: NCT03312166
Status: COMPLETED
Last Update Posted: 2024-09-19
First Post: 2017-10-12
Is Gene Therapy: True
Has Adverse Events: False

Brief Title: Compressive Device to Prevent Keloïd Scars Recurrence [SCARWARS]
Sponsor: Centre Hospitalier Universitaire de Besancon
Organization:

Study Overview

Official Title: First Study Evaluating Efficiency and Safety of a Compressive Device to Prevent Keloid Scars Recurrence After Surgery
Status: COMPLETED
Status Verified Date: 2024-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: SCARWARS
Brief 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.
Detailed Description: None

Study Oversight

Has Oversight DMC: True
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: