Registry for new treatments in patients with atopic dermatitis
Official title: BioDay Registry: Prospective, Observational Data Collection Regarding the Use of New Systemic Treatment Options in Patients with Atopic Diseases in Daily Practice
Run by UMC Utrecht · NCT03549416 · Data updated 2026-11-12
This study is collecting information from people with atopic dermatitis to see how well new treatments work and how they affect other related conditions like food allergies and asthma.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 0 Years and up |
| Sex | All |
| Enrollment | 1200 (estimated) |
| Sponsor | UMC Utrecht Academic / other |
| Locations | 14 sites (Nijmegen, Gelderland and 13 other locations) |
| Status | Recruiting |
| Started | January 1, 2018 |
| Main results expected | December 31, 2028 |
| Study ends | December 31, 2028 |
| Registry record updated | March 28, 2025 |
| Trial ID | NCT03549416 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include both adult and pediatric patients currently receiving new systemic treatments for atopic dermatitis.
✕Probably not a fit
Patients who are unable or unwilling to complete questionnaires will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
The BioDay Registry collects data on the effectiveness and safety of new systemic treatments for atopic dermatitis, including biologics and Janus kinase inhibitors. This observational study involves multiple centers and aims to gather real-world evidence on treatment outcomes and the impact on related atopic conditions such as food allergies and asthma. Patients of all ages receiving these treatments will be invited to participate by completing questionnaires about their experiences.
Why it matters
Potential benefit: If successful, this registry could provide valuable insights that improve treatment strategies for patients with atopic dermatitis.
How similar studies have gone: Other studies have successfully utilized registries to gather real-world data on treatment effectiveness, making this approach promising.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * All adult and paediatric patients treated with new systemic treatments for AD will be asked for participation in the BioDay Registry Exclusion Criteria: * Patients are not eligible for enrolment in case of presumed inability to answer questionnaires or not willing to answer questionnaires and will be excluded.
Where it's running
-
Radboud University Medical Center
Nijmegen, Gelderland, Netherlands Recruiting -
Isala Dermatologisch Centrum
Zwolle, Overijssel, Netherlands Recruiting -
Medisch Centrum Leeuwarden
Leeuwarden, Provincie Friesland, Netherlands Recruiting -
University Medical Center Groningen
Groningen, Provincie Groningen, Netherlands Recruiting -
IJsselland Ziekenhuis
Capelle aan den IJssel, South Holland, Netherlands Recruiting -
University Medical Center Utrecht
Utrecht, Utrecht, Netherlands Recruiting
Show 8 more locations
-
Meander Medisch Centrum
Amersfoort, Netherlands Recruiting -
Reinier de Graaf ziekenhuis
Delft, Netherlands Recruiting -
Catharina ziekenhuis
Eindhoven, Netherlands Recruiting -
Spaarne Gasthuis
Haarlem, Netherlands Recruiting -
Maastricht Univeristy Medical Center
Maastricht, Netherlands Recruiting -
Haga ziekenhuis
The Hague, Netherlands Recruiting -
Diakonessenhuis
Utrecht, Netherlands Recruiting -
St Antonius ziekenhuis
Utrecht, Netherlands Recruiting
Study contacts
- Principal investigator: Marjolein de Bruin-Weller, Md, PhD — UMC Utrecht
- Study coordinator: Marlies de Graaf, MD, PhD
- Email: M.deGraaf-10@umcutrecht.nl
- Phone: +31887571134
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Roflumilast Cream 0.3% for moderate to severe atopic dermatitis in children, adolescents, and adults
A cream called roflumilast 0.3% is tested once daily to see if it helps people with moderate to severe atopic dermatitis, compared to a non-medicated cream, across ages 6 and up.
-
Nocturnal ScratchSense ring: test of automatic scratch detection in adults with itchy skin
This study tests whether the Replior ScratchSense ring can accurately detect and measure nighttime scratching in adults with itchy skin conditions.
-
ADBest TREAT Registry for adults with atopic dermatitis
A registry in Germany is collecting real-world data from adults with atopic dermatitis to see how treatments are used and how the disease affects quality of life.
-
How lebrikizumab affects the skin microbiome and mycobiome in adults with atopic dermatitis
This study looks at whether lebrikizumab changes the skin bacteria, fungi, and specifically Staphylococcus species, in adults with moderate-to-severe atopic dermatitis.
-
QX-4533 safety study in healthy volunteers and people with moderate-to-severe atopic dermatitis
This study tests the safety and tolerability of QX-4533, given as a pill, in healthy adults and in patients with moderate-to-severe atopic dermatitis to see how the drug behaves in the body and what side effects may occur.
-
Tilrekimig for moderate-to-severe eczema in teens and adults
A 52-week study will test tilrekimig against dupilumab and a placebo to see if it helps people 12 and older with moderate-to-severe atopic dermatitis.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.