Cholecalciferol
DrugOther names: Uvedose
NCT Number: NCT02537509
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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Notify Me15 year and older
All sexes
Interventional
Phase 2
Hôpital Saint André, Bordeaux, France
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Other names: Uvedose
Other names: Placebo of Uvedose
Time frame: 2 years
Measurement of PO-SCORAD score
Time frame: 2 years
Measurement of cumulative consumption of topical anti-inflammatory treatments
Time frame: 2 years
Assessment of desease severity by EASI score
Time frame: 2 years
Assessment of desease severity by IGA score
Time frame: 2 years
Assessment of desease severity by SCORAD score
Time frame: 2 years
Assessment of desease severity by POEM score
Time frame: 2 years
Assessment of the quality of life by DLQI score
Time frame: 2 years
Time frame: 2 years
Time frame: 2 years
Time frame: 2 years
Time frame: 2 years
Rennes University Hospital
Other
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
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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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