Clinical Trials Directory

Trials / Completed

CompletedNCT00993005

CICATRIX in the Treatment of Hypertrophic Scars and Keloids Scars

Efficacy of CICATRIX (Asian Gotu Kola or Pennywort) in the Treatment of Hypertrophic Scars and Keloids Scars.

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
90 (estimated)
Sponsor
Catalysis SL · Industry
Sex
All
Age
18 Years – 55 Years
Healthy volunteers
Not accepted

Summary

The purpose of the study is to assess the efficacy of CICATRIX (Asian Gotu Kola or Pennywort) usage in the treatment of Hypertrophic scars and keloids. The duration of this double-blind placebo controlled phase 3 clinical trial will be 12 weeks. The estimated number of persons to be recruited and randomized for the study is 90.

Conditions

Interventions

TypeNameDescription
OTHERCicatrixDosage commensurate with surface to be treated. After washing and drying the affected area, a thin layer of CICATRIX (Topical use) will be applied on the scar rubbing in different directions for 2 minutes, three times a day, for 12 weeks.
OTHERPlaceboDosage commensurate with surface to be treated. After washing and drying the affected area, a thin layer of PLACEBO (Topical use) will be applied on the scar rubbing in different directions for 2 minutes, three times a day, for 4 weeks.

Timeline

Start date
2009-10-01
Primary completion
2010-12-01
Completion
2010-12-01
First posted
2009-10-09
Last updated
2010-12-08

Locations

1 site across 1 country: Cuba

Source: ClinicalTrials.gov record NCT00993005. Inclusion in this directory is not an endorsement.