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Study identifier: NCT03549416 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

BioDay Registry: Data Collection Regarding the Use of New Systemic Treatment Options in Patients with Atopic Dermatitis

Condition: Atopic Dermatitis  ·  Sponsor: UMC Utrecht

PhaseN/A
Planned participants1200
Who can joinAll sexes, 0 Years to no upper limit
Healthy volunteersNo

About this study

The BioDay Registry aims to address the need for daily practice data regarding the effectiveness and safety of new systemic treatment options (like biologics and Janus kinase inhibitors) in patients with atopic dermatitis and effect on other atopic comorbidities in a multicenter setting. The registry already consists of several additional modules concerning atopic comorbidities, like food allergy and asthma, and a module for conjunctivitis during biologic treatment.

This description comes directly from the study's public registry record.

Talk to the study team

Marlies de Graaf, MD, PhD  ·  +31887571134  ·  M.deGraaf-10@umcutrecht.nl

Ilona de Ridder  ·  L.H.deRidder-2@umcutrecht.nl

Always discuss trial participation with your own doctor first.

Locations (14)

Radboud University Medical CenterNijmegen, Gelderland, NetherlandsRecruiting
Isala Dermatologisch CentrumZwolle, Overijssel, NetherlandsRecruiting
Medisch Centrum LeeuwardenLeeuwarden, Provincie Friesland, NetherlandsRecruiting
University Medical Center GroningenGroningen, Provincie Groningen, NetherlandsRecruiting
IJsselland ZiekenhuisCapelle aan den IJssel, South Holland, NetherlandsRecruiting
University Medical Center UtrechtUtrecht, Utrecht, NetherlandsRecruiting
Meander Medisch CentrumAmersfoort, NetherlandsRecruiting
Reinier de Graaf ziekenhuisDelft, NetherlandsRecruiting
Catharina ziekenhuisEindhoven, NetherlandsRecruiting
Spaarne GasthuisHaarlem, NetherlandsRecruiting
Maastricht Univeristy Medical CenterMaastricht, NetherlandsRecruiting
Haga ziekenhuisThe Hague, NetherlandsRecruiting

+ 2 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT03549416