Cicatrix Cream in Post Surgical Scars and Epidermic Burn

Catalysis SL100 enrolled

Overview

The purpose of the study is to assess the effect of CICATRIX (Asian Gotu Kola or Pennywort) usage in the treatment of epidermic burns or post surgical scars. The duration of this phase 2 clinical trial will be two months.

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

100

Conditions

Post Surgical Scars Epidermic Burn

Interventions

Cicatrix creamOTHER

We will be carried out the topical application of the product (Cicatrix cream) in the epidermic burns or post surgical scars by administration fo the patients twice a day during two months to a dose of 0,1 ml of cream for each cm of surface, being controlled by the specialist in biweekly consultations. To the patient will be explained the technique of the application.

Eligibility

Sex: ALLMax age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Patient with lesions characteristic of the investigated illness. * Signed informed consent Exclusion Criteria: * Patient that refer manifestations of high sensibility to the medication or to some of the components of the product * Patient that don't want to participate in the study * Patient not very cooperative * Family responsible not very cooperative

Locations (1)

Juan Manuel Marquez Pediatric Hospital

Havana, La Habana, Cuba

Outcomes

Primary Outcomes

Reduction of the areas of lesions at 2 months (end of the treatment)

Time frame: 2 months

Secondary Outcomes

Coloration of the lesions at 2 months (end of the treatment)

Time frame: 2 months

Adverse effects

Time frame: 2 months

Data from ClinicalTrials.gov

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