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Active, not recruiting Observational

Ocular Comorbidity in Atopic Dermatitis

NCT04973384 · tracked via the Priya Life Science Denmark tracker
Phase
Observational
Started
2021-08-05
Last updated
2024-11-15

Condition(s) studied

Atopic Keratoconjunctivitis

Study summary

A clinical characterization of a large cohort of patients with different severities of AD and ocular symptoms/atopic keratoconjunktivitis (AKC). The data will contribute to assess the frequency of complications in order to give a rationale for focused prevention and treatment strategy.

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Danish talking * Diagnosed with atopic dermatitis (AD) * Current or previous ocular symptoms suspected to be atopic keratoconjunctivitis Exclusion Criteria: * No pause in eyedrops * Ocular infections within the last 3 months * Use of local or systemic antibiotics within the last 3 months * Significant untreated systemic disease such as hypertension, heart failure, diabetes mellitus, previous cerebral infarction or bleeding, lung diseases and autoimmune diseases other than atopic dermatitis and related comorbidities. The diseases are accepted if they are well treated or do not require treatment * Current pregnant or breastfeeding * Use of contact lenses, unless these are paused 2 weeks before the examination or they are due to keratoconus treatment * If the eye symptoms turn out not to be related to atopic keratoconjunctivitis * If it is assessed that the individual cannot participate sufficiently for the examination

Primary outcome measure(s)

  • Bulbar redness (BR) score — 1 day At examination
    Difference in Bulbar redness (BR) score (Keratograph 5M, R-scan). Scale from 0-4. A higher score indicates more severe BR.

Trial sites (1)

FacilityCityRegionStatus
Department of Ophthalmology, Rigshospitalet-Glostrup Glostrup Municipality Denmark
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04973384 on ClinicalTrials.gov ↗ ← All trials in Denmark