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Clinical Trial Summary

Sixty two subjects will take part in this study. The study is unic arm. The subjects used the product once and will be evaluated in the regression of pimples in the times 0,4,6,8 and 24 hours after application.

A follow-up visit will be made 24 hours after initiation of treatment.


Clinical Trial Description

n/a


Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms

  • Acne Vulgaris
  • Treatment of Acne Vulgaris Grade II in a Short Period of Time.

NCT number NCT01260571
Study type Interventional
Source Zurita Laboratorio Farmaceutico Ltda.
Contact Sergio Schalka, Doctor's
Phone (11) 36816362
Email medcin@medcinonline.com.br
Status Not yet recruiting
Phase Phase 4
Start date January 2011
Completion date March 2011