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)

Zurita Laboratorios

Status and phase

Unknown

Phase 4

Conditions

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

Treatments

Drug: Benzoyl peroxide and sulfur

Study type

Interventional

Funder types

Industry

Identifiers

NCT01260571

EAA 554-10/v6

Details and patient eligibility

About

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.

Enrollment

62 estimated patients

Sex

All

Ages

12 to 35 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

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 criteria

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