Contact dermatitis. Unspecified contact dermatitis
Conditions
Interventions
Intervention 1: Intervention group: Patients will receive 30 grams of powder per day, orally, from reputable pharmaceutical companies(half the dose in children) divided into two equal doses. Interven
Sponsors
Shiraz University of Medical Sciences
Eligibility
Sex/Gender
All
Age
5 Years to No maximum
Inclusion criteria
Inclusion criteria: Age over 5 years Contact dermatitis(clinical or with patch test)
Exclusion criteria
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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). | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSeyyed Mohammad Hashemi
Shiraz University of Medical Sciences
Outcome results
None listed