Status:

UNKNOWN

Clinical Study to Evaluate the Efficacy of Topical Medications Containing Benzoyl Peroxide and Sulfur in the Regression in the Short Time (24 Hours) of Moderate Acne Vulgaris Grade II (Pimples)

Lead Sponsor:

Zurita Laboratorio Farmaceutico Ltda.

Conditions:

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

Eligibility:

All Genders

12-35 years

Phase:

PHASE4

Brief 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 ap...

Eligibility Criteria

Inclusion

  • Subjects of both sexes aged to 12 years to 35 years
  • Oily skin prone to acne
  • Presence of at least three inflammatory lesions, diagnosed as grade II acne vulgaris.
  • Sign the informed Consent Form
  • Comply the requirements and attend to study visits

Exclusion

  • Pregnancy (need for urinary pregnancy test for women of childbearing age)
  • Lactation
  • Presence of acne conglobata and nodulocystic
  • Pathologies associated hormonal (thyroid diseases, ovaries micropolycystic)
  • Drug use systemic corticosteroids, anticonvulsants and / or new drugs for up to one month before to selection.
  • History of atopy or allergic cutaneous
  • History of hypersensitivity to benzoyl peroxide and sulfur
  • Beginning or ending the use of contraceptives (for females)
  • Intense sun exposure until one month before the evaluation

Key Trial Info

Start Date :

January 1 2011

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

March 1 2011

Estimated Enrollment :

62 Patients enrolled

Trial Details

Trial ID

NCT01260571

Start Date

January 1 2011

End Date

March 1 2011

Last Update

December 15 2010

Active Locations (1)

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1

Medcin Instituto da Pele

Osasco, São Paulo, Brazil, 06023-000