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Effectiveness of whey proteins for the treatment of atopic dermatitis: A pilot study.

Effectiveness of Glycomax 'trademark' Lactoferrin and bovine whey-derived Ig-rich fraction for the treatment of atopic dermatitis: A pilot study

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12614000635662
Enrollment
45
Registered
2014-06-17
Start date
2014-06-19
Completion date
2015-08-28
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

This project aims to investigate the effectiveness of daily supplementation with Glycomax 'trademark' Lactoferrin and bovine whey-derived Ig-rich fraction on symptoms of atopic dermatitis. The study is a double-blind placebo-controlled parallel trial and consists of two phases, a 56 day supplement period followed by a four week post supplement follow up. The study group will consist of both male and females adults (n=45). Participants will range in age from 18-60 years with a confirmed diagnosis of atopic dermatitis made by a dermatologist.

Interventions

Daily oral supplementation for 56 days with a combined 250mg each of bovine whey derived Glycomax 'trademark' lactoferrin and bovine whey-Ig rich fraction or a Placebo, both in tablet form. Each participant will also be provided with a hypoallergenic sorbolene cream (Dermeze Sensitive Cream) for the relief of dryness as required at their discretion. Supplements and the Dermeze cream will be collected at the end of the study for assessing adherence.

Sponsors

Griffith University
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used) (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

Presence of atopic dermatitis according to physician diagnosis using SCORAD

Exclusion criteria

1 is lactose intolerant 2 consumes fish oil, probiotics, prebiotics, whey protein supplements during the trial period 3 requires insulin use (for treatment of diabetes) 4 has history of liver, kidney or thyroid disease 5 uses anti-inflammatory or immune-modulating medications 6 has heavy alcohol consumption 7 is pregnant or intends to become pregnant

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026