Evaluation of Clinical, Perceived and Instrumental Efficacy of a Scar Gel in Preventing Hypertrophic Scars

Recruiting Phase 1 Phase 2 Interventional Study
Acceptability Study Real-use Conditions Safety and Efficacy Topical Administration Hypertrophic Scars Keloid Scars
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 – 70
Sex
Any
Trial phase
Phase 1/2
Study type
Interventional
Purpose
Prevention
Participants needed
80 (estimated)
Sponsor
Herbarium Laboratorio Botanico Ltda · Industry
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About This Trial

Evaluation of the safety and topical efficacy of a scar gel after 90 days of continuous use, comparing it to a benchmark for preventing hypertrophic scars and improving appearance, hydration and pigmentation.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Participants of both sexes aged between 18 and 70 years; 2. Participants with recent scars (\<30 days); 3. Participants with phototypes III to VI according to the Fitzpatrick scale; 4. Agree to follow the trial procedures and attend the center on the days and times determined…
Contacts

Flávia A. S. Addor

(55) 11 3683-5366

contato@medcinpesquisa.com.br

CONTACT