Cicatrix Cream in Post Surgical Scars and Epidermic Burn

• Register: ClinicalTrials.gov
• Last refreshed on: 17 October 2012
• Main ID: NCT01018589
• Date of registration: 20/11/2009
• Primary sponsor: Catalysis SL
• Public title: Cicatrix Cream in Post Surgical Scars and Epidermic Burn
• Scientific title: Effect the Cicatrix Cream in in Treatment of Post Surgical Scars and and Epidermic Burn.
• Date of first enrolment: September 2009
• Target sample size: 100
• Recruitment status: Completed
• URL: http://clinicaltrials.gov/show/NCT01018589
• Study type: Interventional
• Study design: Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Countries of recruitment

Cuba

Contacts

• Name: Edelisa Moredo Romo, MD
• Affiliation: Juan Manuel Marquez Pediatric Hospital

Key inclusion & exclusion criteria

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



Age minimum: N/A
Age maximum: 18 Years
Gender: Both

Health Condition(s) or Problem(s) studied

Epidermic Burn

Post Surgical Scars

Intervention(s)

Other: Cicatrix cream

Primary Outcome(s)

Reduction of the areas of lesions at 2 months (end of the treatment) [Time Frame: 2 months]

Secondary Outcome(s)

Adverse effects [Time Frame: 2 months]

Coloration of the lesions at 2 months (end of the treatment) [Time Frame: 2 months]

Secondary ID(s)

CAT-0904-CU

Source(s) of Monetary Support

Please refer to primary and secondary sponsors