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Regulatory T-cells in Psoriasis Patients as Targets for Therapy

U

University of Aberdeen

Status

Completed

Conditions

Psoriasis

Treatments

Drug: Dovobet, neotigason, etanercept, adalimumab. infliximab

Study type

Observational

Funder types

Other

Identifiers

NCT01233583
pRGF/009/10

Details and patient eligibility

About

The aim of this study is to understand which therapies will suppress effector cells and promote regulatory T cells and To test whether patients with a better response to therapy and longer psoriasis-free periods develop a higher numerical ratio of regulatory to effectors T-cells and/or regulatory cells more able to suppress the effectors.

Full description

This is an observational study for the effect of different treatment options of psorisis on regulatory T-cells. Patients in whom a decision to treat with one of the following therapies (Dovobet, neotigason, narrow-band UVB and anti TNF alpha therapy) and agreed to take part in the study will be selected. Allocation of different treatments to patients is not part of the study. We will enroll 40 patients with moderate to severe psoriasis in the age range from 18 to 70. patients must be treatment-free for at least 2 weeks for topical application and 4 weeks for systemic treatment of psoriasis. females of child bearing potential must be on reliable contraception. Children below 18 years, patients above 70 years, pregnant and lactating patients and immunosuppressed patients are excluded from this study. Blood and tissue samples will be taken before and after treatment. We will also invite 10 patients who are receiving ellipse excisions of naevi, and who known not to have psoriasis, to provide control samples of distal skin beyond the margins required to demonstrate complete removal and control donation of blood.

Enrollment

38 patients

Sex

All

Ages

18 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • • Male and female patients in the age range from 18 to 70 who are diagnosed with moderate to severe psoriasis.

    • Patients must be treatment free for at least 2 weeks for topical application and 4 weeks for systemic treatment of psoriasis.

    • Women of child bearing potential must be on reliable contraception.

    • Patients in whom a decision to treat with one of the following therapies has already been made based on normal clinical care:

      • Dovobet
      • Neotigason
      • Narrow-band UVB
      • Etanercept
      • Adalimumab
      • Infliximab
    • 10 normal controls

Exclusion criteria

  • • Children below 18 years and patients over 70 years.

    • Pregnant and lactating patients.
    • Patients who are known to have immunosuppressive disease (e.g. HIV) or on any immunosuppressive therapy.

Trial design

38 participants in 4 patient groups

Betamethasone/Calcipotriol (Dovobet)
Description:
patients in whom decision to treat with Dovobet by their dermatologist
Treatment:
Drug: Dovobet, neotigason, etanercept, adalimumab. infliximab
Acitretin (neotigason)
Description:
patients in whom decision to treat with neotigason by their dermatologist
Treatment:
Drug: Dovobet, neotigason, etanercept, adalimumab. infliximab
narrow-band UVB
Description:
patients in whom decision to treat with narrow band UVB by their dermatologist
Treatment:
Drug: Dovobet, neotigason, etanercept, adalimumab. infliximab
Anti TNF-alpha
Description:
patients in whom decision to treat with anti TNF-alpha(adalimumab-etanercept-infliximab) by their dermatologist
Treatment:
Drug: Dovobet, neotigason, etanercept, adalimumab. infliximab

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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