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Human skin barrier recovery

Human skin barrier recovery - HSBR

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON43983
Enrollment
8
Registered
2015-05-13
Start date
2015-10-19
Completion date
Unknown
Last updated
2024-06-11

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

Conditions

atopic ezema skin barrier impairment

Interventions

On a small spot on their underarms the SC of subjects will be partially removed non-invasively by taking 10 tape strips. The subjects will apply 2 g of an emollient enriched with barrier lipids twic

Sponsors

Universiteit Leiden
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - age between 18 and 40. - Caucasian - AE is present for * 2 years - TEWL values before the start of the study are * 15 g/m2/h on non-lesional skin

Exclusion criteria

Exclusion criteria: - Abundant hear, tattoos, or lesions on the underarm - Chronically inflammatory (skin)disease, except AE; - Dermatological disorders or a history of dermatological disorders (not AE); - History of drug abuse; - Pregnancy;

Design outcomes

Primary

MeasureTime frame
The main study parameters and endpoints are: the physical properties of the SC lipid matrix after barrier recovery. These are assessed as, the lipid composition (measured by liquid chromatography/mass spectrometry (LC-MS)) and lipid organization (measured by attenuate total reflectance Fourier transform infrared spectrometry (ATR FTIR)). Another pirmary study parameter is the barrier function of the skin. The transepidermal water loss will be used to determine this. A third primary parameter is the disease severity, for which (local)SCORAD and EASI will be used.

Secondary

MeasureTime frame
n.a.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)