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A randomized, blinded, clinical trial assessing the efficacy of superfine merino wool base layer garments (SMWBG) in children with Atopic Dermatitis (AD) measuring SCORAD, EASI, POEM and DSA scores

A randomized, blinded, clinical trial assessing the efficacy of superfine merino wool base layer garments (SMWBG) in children with Atopic Dermatitis (AD) measuring SCORAD, EASI, POEM and DSA scores

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN53706986
Enrollment
30
Registered
2018-01-20
Start date
2014-06-25
Completion date
Unknown
Last updated
2019-02-11

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

Conditions

Atopic dermatitis Skin and Connective Tissue Diseases Atopic dermatitis

Interventions

A with-garment intervention phase (IP) where participants wore Superfine Marino Wool Base Layer Garments [SMWBG] for 5 weeks, was compared with pre-garment IP and post-garment IP where participant's n

Sponsors

Queensland Institute of Dermatology
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Participant and/or guardian have provided informed consent 2. Participant is of either sex and of any race/ethnicity and aged 6 to 25 years of age, at the time of screening 3. Participant has a diagnosis of dermatitis for at least six months, proven by itchy skin located, but not limited to skin creases (front of elbows, back of knees and around eyes and neck) 4. Participant's dermatitis severity should be stable with no recent hospitalisations, increased systemic steroid use or recurrent clinically significant cutaneous infections within the last 5 weeks prior to screening 5. Participant or guardian must be capable of completing written questionnaires 6. The participant must be capable of completing the procedural requirements of the protocol 7. Optional photographic collection for research purposes

Exclusion criteria

Exclusion criteria: 1. Participation in any clinical trials in the last 30 days prior to screening 2. Participant and or guardian(s) are unable to complete written questionnaires 3. Women of childbearing potential, who are pregnant or breastfeeding or intend to become pregnant (within 2 months of completing the trial) 4. Proven allergic contact dermatitis to merino wool by allergy patch testing 5. Males with a clothing size greater than 2XL as determined by Investigator and/or females with clothing size greater than 18 6. Participant is unable to wear garments for a minimum of 6 hours per day 7. Participant has any kind of disorder that, in the opinion of the Investigator may compromise the ability of the participant or guardian to give informed consent

Design outcomes

Primary

MeasureTime frame
The tolerability of superfine Merino wool base layer garments measured using SCORing Atopic Dermatitis (SCORAD), (Eczema Area and Severity Index), Dermatitis Severity Assessment (DSA), and Patient Orientated Eczema Measure (POEM), during the Pre-Garment intervention Phase (5 week period with 3 visits scheduled including baseline scores), the With-Garment intervention Phase (5 week period with 2 visits scheduled), and the Post-Garment intervention Phase (5 week period with 2 visits scheduled)

Secondary

MeasureTime frame
Quality of life, measured using Dermatology Life Quality Index (DLQI), Childrens Dermatology Life Quality Index (CDLQI), Patient Orientated Eczema Measure (POEM), during the Pre-Garment intervention Phase (5 week period with 3 visits scheduled including baseline scores), the With-Garment intervention Phase (5 week period with 2 visits scheduled), and the Post-Garment intervention Phase (5 week period with 2 visits scheduled)

Countries

Australia

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026