NCT02584010

Efficacy Study of Two Silicon-based Products to Treat Scars

Comparative, Open, Randomized Trial Between Two Silicon-based Products to Treat Postoperative Scars

• Status: Withdrawn
• Phase: N/A
• Study type: Interventional
• Enrollment: 0 (actual)
• Sponsor: Ache Laboratorios Farmaceuticos S.A. · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Accepted

Summary

This study aims to determine if a silicon-based gel and a silicon-based aerosol are effective in the treatment of postoperative scars.

Detailed description

Improve the final aspect of scars, have been a challenge for medicine. Silicon based products have been used in various ways to prevent hypertrophic scars and keloids since 1980. A great percentage of studies shows that silicon-based products improves the aspect of scars in different pathologies. The main objective of this trial is to evaluate the efficacy, using the Vancouver scale, of two silicon-based products (Kelofin gel and Kelofin aerosol) after 180 days. 300 participants that meet all the inclusion criteria and are not classified in any of the exclusion criteria will be randomly allocated to one of thre treatment groups( Kelofin Gel, Kelofin Aerosol and no treatment) of the study.

Conditions

• Scars

Interventions

Type	Name	Description
OTHER	Silicon-based aerosol	Apply twice a day over the postoperative scar
OTHER	Silicon-based gel	Apply twice a day over the postoperative scar

Timeline

• Start date: 2016-01-01
• Primary completion: 2016-07-01
• Completion: 2016-10-01
• First posted: 2015-10-22
• Last updated: 2017-02-15