A randomized, double-blind, vehicle-controlled, half-side comparison, monocenter, clinical study evaluating the efficacy and safety of a herbal dermatitis ointment for the treatment of mild to moderate atopic dermatitis
- Conditions
- atopic dermatitis
- Registration Number
- EUCTR2004-002594-23-DE
- Lead Sponsor
- Weber & Weber GmbH & Co.KG
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- All
- Target Recruitment
- Not specified
Inclusion Criteria
Caucasian males and females betwen 18 and 65 years of age with mild to moderate atopic dermatitis
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range
Exclusion Criteria
Use of glucocorticoids 4 weeks prior to study entry
Systemic use of antihistamines, antipruritics or immunosuppressants 2 weeks prior to study entry
Any treatment of target area for at least 2 weeks prior to study entry
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Main Objective: To evaluate the efficacy and safety of an herbal ointment in mild to moderate atopic dermatitis in adults;Secondary Objective: ;Primary end point(s): Local SCORAD: summary score for erythema, edema/papulation, oozing/crust, excoriation and lichenification (4 point scale)
- Secondary Outcome Measures
Name Time Method