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Evaluation of efficacy of whey protein in contact dermatitis

Not Applicable
Conditions
Contact dermatitis.
Unspecified contact dermatitis
Registration Number
IRCT20190202042587N1
Lead Sponsor
Shiraz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
60
Inclusion Criteria

Age over 5 years
Contact dermatitis(clinical or with patch test)

Exclusion Criteria

Cows milk allergy
Pregnancy or severe disease as malignancy
Patients who had a new treatment or an increase in the dose within 4 weeks prior to the intervention
Patients treated with immunosuppressive drugs

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Reduced scores in questionnaire and during periodic examination, which indicate better control of the disease and reduced symptoms. Timepoint: At the beginning of the study, 14 and 28 days after starting the drug. Method of measurement: Questionnaire including EASI (eczema area and severity index) and VAS (visual analog scale) and DLQ index (dermatology life quality index).
Secondary Outcome Measures
NameTimeMethod
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