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Cicatrix Cream in Cutaneous Groves

Effect the Cicatrix Cream in Cutaneous Groves Treatment

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01018212
Enrollment
50
Registered
2009-11-23
Start date
2009-09-30
Completion date
2010-12-31
Last updated
2010-12-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cutaneous Groves

Keywords

Cutaneous Groves

Brief summary

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.

Interventions

We will be carried out the topical application of the product (Cicatrix cream) in the lesions auto administration three times a day during four months, being controlled by the specialist in months consultations. The dose of 0,1 ml of cream for each cm. of surface, To the patient will be explained the technique of the application.

Sponsors

Catalysis SL
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
10 Years to 18 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frame
They are the cutaneous grooves, being Observed the reduction of the number of the lesions monthly.4 month

Secondary

MeasureTime frame
Extension of the groves and the reduction of these expressed in centimetres4 months
Adverse effects4 months

Countries

Cuba

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026