MedPath

Cicatrix Cream in Post Surgical Scars and Epidermic Burn

Phase 2
Completed
Conditions
Post Surgical Scars
Epidermic Burn
Interventions
Other: Cicatrix cream
Registration Number
NCT01018589
Lead Sponsor
Catalysis SL
Brief Summary

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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
100
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
ACicatrix creamCicatrix cream
Primary Outcome Measures
NameTimeMethod
Reduction of the areas of lesions at 2 months (end of the treatment)2 months
Secondary Outcome Measures
NameTimeMethod
Coloration of the lesions at 2 months (end of the treatment)2 months
Adverse effects2 months

Trial Locations

Locations (1)

Juan Manuel Marquez Pediatric Hospital

🇨🇺

Havana City, Havana, Cuba

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