Skip to content

Effects of visible light on inflammation and skin barrier recovery following acute perturbation

Effects of visible light on inflammation and skin barrier recovery following acute perturbation - Effect of visible light on skin barrier recovery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON43517
Enrollment
44
Registered
2016-07-20
Start date
2016-11-14
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

skin barrier stratum corneum

Interventions

None listed

Sponsors

Philips Research
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. skin type I, II or III (Fitzpatrick scale); 2. 18 - 40 years old; 3. willing to give written informed consent

Exclusion criteria

Exclusion criteria: 1. diagnosis of histamine hypersensitivity; 2. presence of cardiac pacemakers or other implanted electric devices; 3. pregnancy or lactation; 4. atopic predisposition (i.e. allergy, atopic/contact dermatitis, hay fever, asthma); 5. any current (skin) disease including conditions causing photosensitivity; 6. predisposition to respond allergic; 7. use of immunosuppressive drugs; 8. use of antihistamines drugs; 9. use of medication for hypertension with airway constricting activity; 10. use of medication with photosensitizing effects; 11. skin type IV, V, VI (Fitzpatrick scale); 12. excessive sun exposure or tanning less than 2 weeks before the beginning of the study.

Design outcomes

Primary

MeasureTime frame
The main study parameters are the recovery of the skin barrier after tape stripping, measured with transepidermal water loss (marker of skin barrier status), and the clearance of inflammation after histamine iontophoresis, measured with a* value (marker of skin redness). Both measurements are non-invasive. Tape stripping and histamine iontophoresis will be performed twice on the same volunteer, on two consecutive weeks. On one occasion stimulation is followed by irradiation, in the other no irradiation is performed serving as control.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)