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CompletedNCT02599415Updated Mar 25, 2016

Anti-psoriatic Effect of TL01 Light Therapy

An interventional study of TL01 light treatment in Psoriasis, sponsored by University of Aberdeen. Completed at 1 site in United Kingdom. Open to participants aged 18 Years to 70 Years. Per ClinicalTrials.gov, last updated 2016-03-25.

Sponsored by University of Aberdeen · Not applicable, Interventional, and Diagnostic

Phase
Not applicable
Study type
Interventional
Enrollment
6
Allocation
Not applicable
Ages
18 Years to 70 Years
Sex
All
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Study summary

This is a pilot study to investigate the effect of TL01 narrow band UVB therapy on the resident dermal dendritic cells characterized by expression of CD1c and CD141. These cells were reported to have a role in induction of tolerogenic regulatory T cells and production of IL-10. The investigators proposed to investigate the effect of NB-UVB on these subsets of cells after two weeks of treatment to provide better understanding of the mechanism of action of light treatment.

Read the detailed description

Six patients with plaque psoriasis were recruited from the phototherapy unit. These patients were referred by their dermatologist to receive narrow-band UVB (TL01) light treatment. Two 6 mm lesional skin punch biopsies were taken at baseline and 2 weeks after commencing the light treatment to study the effect of light on innate immune cells involved in psoriasis pathogenesis.

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Conditions studied

  • Psoriasis

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Keywords

  • psoriasis patients referred to receive TL01 NB-UVB therapy
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In context

Psoriasis

1,928 studies on the registry are indexed under Psoriasis; 234 are open to participants now.

This study's enrollment of 6 is below the median of 70 across 1,472 interventional studies indexed under Psoriasis.

Browse Psoriasis studies →

Lead sponsor

University of Aberdeen is the lead sponsor of 175 studies on the registry; 23 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Male and female psoriasis patients in whom the decision to treat with NB-UVB therapy, as part of their routine clinical care, has been taken by their dermatologist in the age range of 18-70 years.

Exclusion criteria

Exclusion Criteria:

  • patients currently on antipsoriatic treatment.

    • Patients with immunosuppressive diseases
    • Patients on immunosuppressive therapies
    • Pregnant or lactating female patients
    • Patients unable to provide a written consentProcedure
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Study design

Phase
Not applicable
Primary purpose
Diagnostic
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
6 participants (actual)

Study arms

  • Other
    TL01 light treatment

    routine treatment with a CE marked device that has been used for this disease for many years

    Device: TL01 light treatment

Interventions

  • DeviceTL01 light treatment

    Patients received treatment in TL01 cabinet three sessions weekly according to a standard escalating protocol based on minimal erythema dose. Standard dose ranges between 0.55 and 3.13J/cm2.

    Also known as: Waldmnn Gmbh cabinet

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What researchers measure

Primary outcomes

  1. determination of the effect of TL01 NB-UVB on numbers of CD1c and CD141 cells

    no adverse events recorded after two weeks of TL01 treatment

    Time frame: 3 months

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Study locations

1 site
  • University of Aberdeen
    Aberdeen, AB25 2zb, United Kingdom
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 25, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02599415
Collaborators
NHS Grampian
Responsible party
Sponsor
First posted
Nov 6, 2015
Start date
Sep 2014
Primary completion
Dec 2014
Completion
Dec 2014
Last update
Mar 25, 2016

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2016. You cannot join it, but the record below documents what was studied.

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