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Narrowband Ultraviolet B Versus Narrowband Ultraviolet B Plus Ultraviolet A1 for Atopic Eczema

Not Applicable
Completed
Conditions
Atopic Eczema
Interventions
Radiation: combined ultraviolet phototherapy (NB-UVB + UVA1) vs. NB-UVB monotherapy
Registration Number
NCT02915146
Lead Sponsor
University of Dundee
Brief Summary

Narrowband ultraviolet B phototherapy is the "standard" phototherapy for atopic eczema; ultraviolet A1 is sometimes used but is not a widely available treatment. We do not know the most important chromophores in treating atopic eczema; in which phototherapy is thought to work by improving epidermal barrier function, having beneficial effects on skin microbiome and local immunosuppression. It seems plausible that there are several chromophores and that 'targetting' several at once with different wavebands should help and for severe eczema that has not responded adequately to narrowband UVB or ultraviolet A1 alone the combination is sometimes used. This study is to test if the combination is moderately to greatly more effective than narrowband ultraviolet B monotherapy amongst patients referred for any form of first-line phototherapy for atopic eczema.

Detailed Description

Narrowband ultraviolet B phototherapy is the "standard" phototherapy widely used for atopic eczema; ultraviolet A1 is sometimes used but is not a widely available treatment. We do not know the most important chromophores in treating atopic eczema; in which phototherapy is thought to work by improving epidermal barrier function, having beneficial effects on skin microbiome and local immunosuppression.

It seems plausible that there are several chromophores (the molecules that absorb the ultraviolet photons to set in chain the effects we are aiming for) and that 'targetting' several chromophores at once with different wavebands should help. For severe eczema that has not responded adequately to narrowband UVB or ultraviolet A1 alone the combination is sometimes used in the few centres where UVA1 is available.

This study is to test if the combination is moderately to greatly more effective than narrowband ultraviolet B monotherapy amongst patients referred for any form of first-line phototherapy for atopic eczema.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
39
Inclusion Criteria
  • Patients with atopic eczema as diagnosed by a dermatologist, defined according to the UK Working Party diagnostic criteria, considered for any form of whole body phototherapy
  • Age 12 years and above
  • Able to understand and comply with protocol requirements and treatment visits, instructions and protocol stated restrictions
  • Provision of written informed consent in accordance with the Scottish Children's Network consent guidance and standard operating procedure (SOP) for subjects aged 12-15 years
  • Provision of written informed consent (subjects age 16 years and over)
Exclusion Criteria
  • Unable to provide written informed consent in accordance with the Scottish Children's Network consent guidance and SOP
  • Unable to provide written informed consent (subjects age 16 years and over)
  • Currently being treated, or treated within the past 2 weeks, with systemic immunosuppressive therapy
  • Current use of drugs known to cause photosensitivity
  • Phototherapy, photochemotherapy, or sunbed use in the preceding 3 months
  • Known abnormal photosensitivity
  • Previous history of skin cancer
  • Participation in another research study within the past three months

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
NB-UVB + UVA1combined ultraviolet phototherapy (NB-UVB + UVA1) vs. NB-UVB monotherapyNarrowband ultraviolet B combined with ultraviolet A1 phototherapy will be used
NB-UVB monotherapycombined ultraviolet phototherapy (NB-UVB + UVA1) vs. NB-UVB monotherapyNarrowband ultraviolet B monotherapy will be used
Primary Outcome Measures
NameTimeMethod
Change in EASI (eczema severity score) - proportions reaching 50% reductionFrom beginning to end of treatment (25 weeks)

observer-assessed eczema severity

Secondary Outcome Measures
NameTimeMethod
POEM (patient orientated eczema measure)26 weeks after treatment completion

patient-assessed eczema severity

Trial Locations

Locations (1)

Ninewells Hospital

🇬🇧

Dundee, United Kingdom

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