Subject Reported Target-lesion Numeric Rating Scale Evaluation by Subjects With Plaque Psoriasis Treated With Clobex® (Clobetasol Propionate) Spray 0.05%
Status: | Completed |
---|---|
Conditions: | Psoriasis |
Therapuetic Areas: | Dermatology / Plastic Surgery |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 10/19/2013 |
Start Date: | July 2013 |
End Date: | September 2013 |
Contact: | Warren J Winkelman, MD |
Email: | warren.winkelman@galderma.com |
Phone: | 817-961-5494 |
The aim of this study is to investigate the utility of a technological based rating scale
for assessing improvement in plaque psoriasis with Clobex spray treatment.
Inclusion Criteria:
- Subjects 18 years of age or older.
- Subjects with a board certified dermatologist clinical diagnosis of active moderate
to severe psoriasis lesions affecting up to 20% of the body surface area at the
baseline visit, and in the opinion of the investigator, is otherwise a good candidate
for treatment with clobetasol propionate 0.05% spray.
- Subjects with a target lesion of at least 1 cm x 1 cm
- Subjects who agree to be photographed at each visit
Exclusion Criteria:
- Subjects with any condition or presentation that may, in the opinion of the
investigator, may put the subject at risk, may confound study results, or may
interfere with participation in the study.
- Subjects with any known allergies to any of the ingredients listed on the test
article label or surgical ink.
- Subjects who are pregnant or breast-feeding, or who plan to become pregnant or breast
feed during the course of the trial.
- Subjects that are relatives of the investigator, or are themselves or a relative of
any study staff or any Galderma employee.
- Subjects who have participated in an investigational study within 30 days of
enrollment; participated in biologic investigational studies within 90 days of
enrollment, or subjects planning to participate in any other interventional clinical
research study while enrolled in this trial.
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