Cicatrix Cream in Cutaneous Groves

Catalysis SL

Status and phase: Completed; Phase 2

Conditions: Cutaneous Groves

Treatments: Other: Cicatrix cream

Study type: Interventional

Funder types: Industry

Identifiers

NCT01018212

CAT-0902-CU

Details and patient eligibility

About

The purpose of the study is to assess the effect of CICATRIX (Asian Gotu Kola or Pennywort) usage in the treatment of cutaneous grooves. The duration of this phase 2 clinical trial will be 4 months.

Enrollment: 50 estimated patients

Sex: All

Ages: 10 to 18 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• 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.
• Responsible family not very cooperative.

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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50 participants in 1 patient group

A

Experimental group

Description:

Cicatrix cream

Treatment:

Other: Cicatrix cream