Clinical Trials Directory

Trials / Completed

CompletedNCT01229085

Efficacy Study of the Combination Mometasone + Salicylic Acid in Patients With Psoriasis

CLINICAL ASSESSMENT OF THE EFFECTIVENESS OF ASSOCIATION MONETASONE FUROATE 0.1% SALICYLIC ACID AND 5% FOR SUBMISSION OF OINTMENT TOPICAL DERMATOLOGICAL USE OF LABORATORY Glenmark Pharmaceuticals Ltd, IN PATIENTS WITH PSORIASIS.

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
71 (actual)
Sponsor
Azidus Brasil · Industry
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

To evaluate the efficacy of the combination of mometasone furoate 0.1% and Salicylic Acid 5% in patients of both sexes who presented clinical symptoms of psoriasis of mild to moderate.

Detailed description

Phase III clinical trial, systematic sampling, open-label study that evaluated the efficacy of the combination of mometasone furoate 0.1% and 5% salicylic acid in 71 patients with lesions of mild to moderate psoriasis treated for up to 45 days or less than this, at the discretion of the investigator. The results were statistically analyzed and investigational data and their conclusions are referred to in this report.

Conditions

Interventions

TypeNameDescription
DRUGmemotasone + salicylic acidmometasone 0,1% + salicylic acid 5%.

Timeline

Start date
2006-09-01
Primary completion
2007-10-01
Completion
2007-10-01
First posted
2010-10-27
Last updated
2010-10-27

Locations

1 site across 1 country: Brazil

Source: ClinicalTrials.gov record NCT01229085. Inclusion in this directory is not an endorsement.