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UnknownNCT01024374

Evaluation of the Effectiveness of a Product Containing Topical Hydrocortisone in the Treatment of Seborrheic Dermatitis of the Face

Avaliação da eficácia de um Produto de Uso tópico Contendo Hidrocortisona no Tratamento de Dermatite seborréica na Face.

Status
Unknown
Phase
Study type
Observational
Enrollment
60 (estimated)
Sponsor
Allergisa Pesquisa Dermato-Cosmetica LTDA · Industry
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Accepted

Summary

Clinical single-blind randomized comparison with the overall objective of evaluating the clinical efficacy of the products Nutracort lotion and Nutracort cream in the treatment of seborrheic dermatitis on the face. Will be held clinical and perceived efficacy assessment and instrumental measurements. Each product will be applied at half face for 7 consecutive days and all applications will be monitored in the research site. 60 volunteers will be recruited. Evaluations will be held at the following times: T0 - before the initial application of the product; T1 - 24 hours after starting treatment, T2 - 48 hours after starting treatment, T3 - 72 hours after initiation of treatment, T4 - 96 hours after the start treatment, T7 - 7 days after initiation of treatment.

Conditions

Timeline

Start date
2010-04-01
First posted
2009-12-02
Last updated
2009-12-02

Source: ClinicalTrials.gov record NCT01024374. Inclusion in this directory is not an endorsement.

Evaluation of the Effectiveness of a Product Containing Topical Hydrocortisone in the Treatment of Seborrheic Dermatitis (NCT01024374) · Clinical Trials Directory