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NCT Number: NCT02537509

PRAgmatic Trial in Atopic Dermatitis Testing Long-term Control Effectiveness of New Phototherapy Regimen During Winter Coupled With Oral Vitamin D Supplementation vs. Placebo

Spaced phototherapy sessions during winter as add-on therapy in combination with vitamin D supplementation or not, could be beneficial to improve disease LTC in AD patients

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Key information

Age range

15 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Hôpital Saint André, Bordeaux, France

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About this study

The major therapeutic challenge in patient with Atopic Dermatitis is long-term control of disease activity (LTC), for which the current TAT-based pro-active strategy does not meet all the needs.

Phototherapy is a good candidate: it is widely used as a second-line treatment in AD with demonstrated efficacy. However, only short-term control has been evaluated; and only 2-3 times a week intensive schedules have been tested and are used in current practice. A novel phototherapy regimen would be required for disease LTC, allowing a trade-off between disease control, UV-induced risks, and patient adherence.

Vitamin D supplementation is another good candidate: several studies have shown lower serum levels of vitamin D to be correlated with more severe AD; and three short-term, low-power low-quality, placebo-controlled randomised trials testing vitamin D supplementation yielded conflicting results, leaving its therapeutic efficacy undecided for short-term control, and unknown for LTC.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with atopic dermatitis (Hanifin and Rajka criteria),
  • Aged 15 years or more,
  • With > 2 years of disease evolution,
  • With moderate-to-severe disease (IGA > 2),
  • Patients that have received TAT for at least 12 weeks and have symptoms requiring an increase in therapy,
  • Seasonality in disease severity (based on a questionnaire assessing disease improvement during summer),
  • Easy access to a phototherapy cabin (widely implanted in primary care dermatology private practice in France),
  • Effective contraception to be used at least 30 days before initiation of treatment, during treatment and 29 weeks after last administration for women of reproductive age,
  • Written informed consent of the patient
  • For patients aged between 15 and 18, written informed consent of the parents and of the teenager.

Exclusion criteria

  • Any cause of contra-indication for vitamin D supplementation: flare of granulomatosis, primary hyperparathyroidism,
  • Clinical suspicion of hypercalciuria,
  • Indication to a systemic immunosuppressant in the next 2 years,
  • Atopic dermatitis known to be aggravated by UV exposure,
  • Any contra-indication for artificial or solar exposure including: genetic diseases with a predisposition to skin cancer, any history of personal skin cancer (melanoma, squamous cell skin cancer, basal cell skin cancer), lupus, dermatomyositis, any other photosensitizing skin disease, photosensitizing medication (see appendix 2),
  • More than 100 previous phototherapy sessions in lifetime,
  • Pregnancy or breastfeeding,
  • Persons subject to major legal protection (safeguarding justice, guardianship, trusteeship), persons deprived of liberty.

Treatment and study plan

Cholecalciferol

Drug

Other names: Uvedose

Placebo of cholecalciferol

Drug

Other names: Placebo of Uvedose

Primary outcomes

  1. Hierarchical criterion based on repeated measures of PO-SCORAD severity score

    Time frame: 2 years

    Measurement of PO-SCORAD score

  2. Hierarchical criterion based on cumulative consumption of topical anti-inflammatory treatments (collected tubes) during winter

    Time frame: 2 years

    Measurement of cumulative consumption of topical anti-inflammatory treatments

Secondary outcomes

  1. Assessment of desease severity

    Time frame: 2 years

    Assessment of desease severity by EASI score

  2. Assessment of desease severity

    Time frame: 2 years

    Assessment of desease severity by IGA score

  3. Assessment of desease severity

    Time frame: 2 years

    Assessment of desease severity by SCORAD score

  4. Assessment of desease severity

    Time frame: 2 years

    Assessment of desease severity by POEM score

  5. Assessment of the quality of life

    Time frame: 2 years

    Assessment of the quality of life by DLQI score

  6. Measurement of serum Vitamin D (25-(OH)-vitamin D)

    Time frame: 2 years

  7. Measurement of total IgE serum

    Time frame: 2 years

  8. Assessement of number of weeks of well-controlled atopic dermatitis

    Time frame: 2 years

  9. Assessment of inter-visit cumulative consumption of topical anti-inflammatory treatments

    Time frame: 2 years

  10. Assessment of patient satisfaction

    Time frame: 2 years

Sponsors and collaborators

Lead sponsor

Rennes University Hospital

Other

Registry information

Official study title

Multicentre, Cross-over, PRAgmatic Trial in Atopic Dermatitis Testing Long-term Control Effectiveness of New Phototherapy Regimen During Winter as an add-on Therapy, Coupled With Oral Vitamin D Supplementation vs. Placebo in a Randomised, Parallel-group Trial

Acronym: PRADA

Important dates

Study start
2015
Primary completion
2023
Study completion
2023
First posted
Sep 1, 2015
Registry last updated
Mar 23, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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