Scalp Psoriasis Clinical Trial
Official title:
Topical Treatment of Scalp Psoriasis With the Fixed Combination of Calcipotriol and Betamethason (Xamiol® Gel)
Verified date | September 2010 |
Source | LEO Pharma |
Contact | n/a |
Is FDA regulated | No |
Health authority | Germany: Federal Institute for Drugs and Medical Devices |
Study type | Observational |
This non-interventional, prospective, non-controlled study of Xamiol® Gel, a fixed combination of calcipotriol and betamethason dipropionate, shall investigate in daily routine the efficacy, tolerability and changes in quality-of-life parameters in patients with scalp psoriasis
Status | Completed |
Enrollment | 724 |
Est. completion date | May 2010 |
Est. primary completion date | May 2010 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Patients with scalp psoriasis if a treatment with Xamiol® gel is planned anyway Exclusion Criteria: - Contraindications of Xamiol® Gel listed in the German package insert - Pretreatment with Xamiol® within the last 4 weeks - Systemic treatment of psoriasis - UV light therapy |
Observational Model: Cohort, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
Germany | University Clinical Schleswig-Holstein, Campus Kiel | Kiel |
Lead Sponsor | Collaborator |
---|---|
LEO Pharma |
Germany,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Physician's Global Assessment of scalp psoriasis | After approximately 4 weeks | No | |
Secondary | Patient's Quality of Life | After approximately 4 weeks | No |
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