Clinical Trials Directory

Trials / Completed

CompletedNCT00753805

Dietetic Effects of Mare's Milk in Patients With Atopic Dermatitis

Dietetic Effects of Oral Intervention With Mare's Milk on the SCORAD, Faecal Microbiota and Immunological Parameters in Patients With Atopic Dermatitis

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
23 (actual)
Sponsor
University of Jena · Academic / Other
Sex
All
Age
18 Years – 54 Years
Healthy volunteers
Not accepted

Summary

The study was performed to investigate the effects of mare's milk on SCORAD, faecal microbiota and immunological parameters in patients with atopic dermatitis.

Detailed description

Mare's milk has been used in the treatment of inflammatory illnesses for centuries since it was known to contain antimicrobial, anti-inflammatory and immunomodulatory substances. The aim of this study was to examine whether the consumption of mare's milk by patients with atopic dermatitis (AD) has a beneficial effect. As a precondition for participating in this study, the subjects were provided information in writing and verbally about the details of the study. Informed consent was obtained from all volunteers. Before the beginning of the study, all participants were subject to a medical examination in the Clinic for Dermatology and Dermatologic Allergology of the Friedrich Schiller University Jena. The AD was diagnosed according to the atopy-score of Diepgen. Severity of eczema was evaluated by using the SCORAD score. A skin prick test was performed for the exclusion of type 1 sensitivity to mare's milk. The study was designed as a double blind, placebo-controlled crossover trial. Twenty-three patients received 250-ml mare's milk or placebo orally for 16 consecutive weeks. Between the two intervention periods, a four week wash-out period without drinking any test substances was introduced. The intensity of AD was examined using the Severity Scoring of Atopic Dermatitis (SCORAD), which was determined at the start of the study and after 4, 8, 12 and 16 weeks of each intervention period. Blood samples were taken at the start of the study and subsequently after 8 and 16 weeks. Fresh stool samples were taken at the beginning of the study and at the end of each intervention period.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTmare's milkThe participants received 250 ml mare's milk or placebo daily. The placebo drink was based on a hypoallergenic infant formula.

Timeline

Start date
2004-08-01
Primary completion
2005-07-01
Completion
2005-07-01
First posted
2008-09-17
Last updated
2008-09-17

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT00753805. Inclusion in this directory is not an endorsement.