Oregano Ointment vs. Standard Treatment for Pediatric Atopic Dermatitis

• Status: Terminated
• Trial end date: 2017-01-01
• Target enrollment: 0
• Participant gender: All

Summary

This study is designed to evaluate and compare the efficacy of 3% oregano extract ointment prepared in aqueous solution versus 1% hydrocortisone ointment, a standard treatment, in decreasing the inflammation associated with mild to moderate atopic dermatitis. We plan to recruit 40 patients on the ages comprised between 2 and 17 years old and the study duration for each of the patient is 1 month.

• Phase: N/A
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Rutgers, The State University of New Jersey
• Treatments: Cortisol succinate; Hydrocortisone; Hydrocortisone 17-butyrate 21-propionate; Hydrocortisone acetate

Criteria

Inclusion Criteria:

• Male or non-pregnant female subjects aged 2-17 years of age.

• Individuals must be diagnosed with acute-subacute AD regardless of the study.

• Written informed consent must be obtained from all patients or caregivers.

• Women of childbearing potential (WOCBP) must be willing to practice effective contraception for the duration of study treatment.

• Subjects must be willing and able to comply with study conditions, properly apply or have caregivers apply topical medications to the selected body sites, as well as return to the clinic for required visits.

• Subject caregivers must be willing and able to perform ADQ assessment test.

Exclusion Criteria:

• Individuals who are immune-compromised or suffering from infectious disease, malignant disease, are known to be HIV+ or present with a general reduced level of health.

• Individuals diagnosed with underlying dermatological conditions in addition to AD.

• Individuals with a chronic pre-existing disease such as diabetes mellitus or others that in the opinion of the investigator would preclude their participation in the study.

• Individuals who are pregnant, nursing mothers, or subjects planning a pregnancy during the course of the study.

• Subjects/caregivers who are unable to communicate or comply with study conditions due to language disability, poor mental development, or impaired cerebral function.

• Individuals who are simultaneously enrolled in another clinical drug or device research study.

• Individuals with a history of chronic steroid use.

• Individuals needing to concurrently use topical agents, medicinal products containing corticosteroids, or immunosuppressants.

• Individuals who have received systemically administered corticosteroids and/or antihistamines 2 weeks prior to the start of study.

• Individuals undergoing light therapy.

• Individuals who have been treated with another investigation device or drug within 30 days prior to study enrollment.

• Individuals with a known allergy to oregano.