Overview

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

Status:
Completed
Trial end date:
2007-10-01
Target enrollment:
0
Participant gender:
All
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.
Phase:
Phase 3
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Azidus Brasil
Treatments:
Mometasone Furoate
Salicylates
Salicylic Acid
Criteria
Inclusion Criteria:

- Adults of both sexes, regardless of color or social class;

- Age 18 or older, with good mental health;

- Psoriasis patients with mild to moderate;

- Patients who agreed to participate and signed the

- Clarified (appendix);

- Patients who agreed to return for follow-up visits.

Exclusion Criteria:

- Patients who were making use of biologics, corticosteroids or nonsteroidal
anti-inflammatory and non-steroid, or who made use of these topical medications until
15 days before inclusion or 30 days before inclusion when the administration was
orally;

- Patients who were exposed to the sun 15 days before the study began or during the
course of the same;

- Patients who were making use of acetaminophen;

- Patients who did not agree to the terms described in the IC informed consent, -
Patients who also had psoriatic plaques of skin disorders caused by fungi or bacteria
and they were making use of antibiotic or antifungal;

- Lions and other types of skin damage that was not psoriasis;

- Pregnant and nursing women;

- Patients using oral anticoagulants.