The UPDATE Trial (Uvb Phototherapy in Dermatology for ATopic Eczema)

Last updated: August 6, 2024
Sponsor: Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Overall Status: Active - Recruiting

Phase

N/A

Condition

Hives (Urticaria)

Rosacea

Skin Infections/disorders

Treatment

Optimal topical therapy

NB-UVB phototherapy

Clinical Study ID

NCT05704205
NL81882.018.22
  • Ages > 18
  • All Genders

Study Summary

The goal of this randomized controlled trial is to study the (cost)effectiveness of NB-UVB phototherapy in patients with atopic eczema/atopic dermatitis.

Half of the participants will undergo a course of NB-UVB phototherapy of 8-16 weeks and apply optimal topical therapy (OTT) for a minimum of 3 months. Researchers will compare the outcomes of this group with the other half of participants that apply OTT only.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Adult (≥18 years of age) patient meeting the UK working party criteria for atopiceczema;

  • AE insufficiently controlled by standard topical care and therefore eligible forNB-UVB or OTT;

  • Investigator Global Assessment (IGA, 0-4) of ≥ 2 (moderate disease);

  • Eczema Area and Severity Index (EASI) of ≥ 7 (moderate disease);

  • Understood and voluntarily signed and dated an informed consent form prior to anystudy-related procedure or has a legal representative who has, and is willing tocomply with the study's requirements.

Exclusion

Exclusion Criteria:

  • Contra-indication for NB-UVB;

  • Genetic defects associated with photosensitivity or skin cancer;

  • Heavily photo-damaged skin;

  • History of multiple (>1) skin malignancies;

  • Use of systemic immunosuppressants/immunomodulators;

  • Use of medication associated with photosensitivity;

  • Patient is already on systemic AE therapy;

  • Patient is already on OTT in the past 2 months;

  • NB-UVB or any systemic therapy in the past 9 months.

Study Design

Total Participants: 316
Treatment Group(s): 2
Primary Treatment: Optimal topical therapy
Phase:
Study Start date:
February 22, 2023
Estimated Completion Date:
December 31, 2026

Study Description

Atopic eczema (AE) is a chronic fluctuating dermatological disease characterized by a pruritic inflammation of the skin. The condition poses a high global (financial) burden. One of the therapeutic options of AE is phototherapy, with narrowband UVB (NB-UVB) being the most common. The evidence of the (cost-)effectiveness of NB-UVB, however, is scarce and of low quality.

The objective of this pragmatic multicenter single blinded randomized controlled trial is comparing the effectiveness and cost-effectiveness of narrowband ultraviolet B with optimal topical therapy (NB-UVB+OTT) versus OTT at 3 months in adult patients with insufficient control of their AE with standard topical treatment, for whom dermatologist and patient jointly believe that NB-UVB or OTT is needed.

Participants that are randomized into the NB-UVB+OTT group will receive an NB-UVB course (at home or at the outpatient clinic) for at least 8 and up to 16 weeks, combined with OTT for at least 3 months. Participants in the control group (OTT group) will apply OTT for at least 3 months. Visits will occur at baseline and 1-3-6-9-12 months after start. At baseline, patient information is collected including an evaluation of medical history and a physical examination to assess Fitzpatrick skin type and physician-reported clinical signs. During each visit patients are asked to fill out questionnaires. Risks are expected to be as in daily practice.

Primary study parameters/outcome of the study is the percentage of patients with EASI50 (a decrease of the Eczema Area and Severity Index of 50%) at 3 month follow-up. Secondary study parameters/outcome of the study include delta EASI, physician-reported clinical signs, patient-reported symptoms, quality of life, long-term control, cost-effectiveness, side effects at 1-3-6-9-12 months, quantity and potency topical steroid usage, time to starting systemic therapy, patient satisfaction with received treatment, percentage of patients reaching Treatment Target goals and percentage of drop-outs with reasons at 3-6-9-12 months.

Connect with a study center

  • Flevoziekenhuis

    Almere, Flevoland 1315RA
    Netherlands

    Active - Recruiting

  • Medisch Centrum Leeuwarden

    Leeuwarden, Friesland 8934 AD
    Netherlands

    Active - Recruiting

  • Jeroen Bosch Ziekenhuis

    Den Bosch, Noord-Brabant 5223 GZ
    Netherlands

    Active - Recruiting

  • Centrum Oosterwal

    Alkmaar, Noord-Holland 1817 MS
    Netherlands

    Active - Recruiting

  • Amsterdam Universitair Medische Centra

    Amsterdam, Noord-Holland 1105 AZ
    Netherlands

    Active - Recruiting

  • Huid Medisch Centrum

    Amsterdam, Noord-Holland 1105 BJ
    Netherlands

    Active - Recruiting

  • OLVG

    Amsterdam, Noord-Holland 1061 AE
    Netherlands

    Active - Recruiting

  • Bergman Clinics

    Haarlem, Noord-Holland 2015 BJ
    Netherlands

    Active - Recruiting

  • Spaarne Gasthuis

    Hoofddorp, Noord-Holland 2134 TM
    Netherlands

    Active - Recruiting

  • Dijklander Ziekenhuis

    Purmerend, Noord-Holland 1441 RN
    Netherlands

    Active - Recruiting

  • Isala Klinieken

    Zwolle, Overijssel
    Netherlands

    Active - Recruiting

  • Meander Medisch Centrum

    Amersfoort, Utrecht 3813 TZ
    Netherlands

    Active - Recruiting

  • Reinier de Graaf Gasthuis

    Delft, Zuid-Holland 2625 AD
    Netherlands

    Active - Recruiting

  • Leids Universitair Medisch Centrum

    Leiden, Zuid-Holland 2333 ZA
    Netherlands

    Active - Recruiting

  • Alrijne Ziekenhuis

    Leiderdorp, Zuid-Holland
    Netherlands

    Site Not Available

  • Erasmus Medisch Centrum

    Rotterdam, Zuid-Holland 3015 GD
    Netherlands

    Active - Recruiting

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