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Observation of changes in ocular findings before and after the use of the IL-4 and 13 antibody preparation dupilumab

Observation of changes in ocular findings before and after the use of the IL-4 and 13 antibody preparation dupilumab - dupilumab

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000038675
Enrollment
150
Registered
2019-11-26
Start date
2020-03-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atopic dermatitis, bronchial asthma, sinusitis, and ocular disorders

Interventions

None listed

Sponsors

Keio University
Lead Sponsor
Tsurumi University School of Dental Medicine
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All patients using dupilumab who have accepted ophthalmologic examinations and this study

Exclusion criteria

Exclusion criteria: Patients who have refused to provide clinical information to this study

Design outcomes

Primary

MeasureTime frame
Visual acuity, intraocular pressure, refractive value, corneal curvature radius, axial length, Schirmer test, fluorescein score, Rose Bengal or Lissaing Lean score, tear film breakup time, subjective symptom OSDI, optic nerve flicker, imaging findings, blood sampling test, tear fluid, cytology, etc.

Countries

Japan

Contacts

Public ContactEisuke Shimizu

Department of Ophthalmology, Keio University School of Medicine Ophthalmology

ophthalmolog1st.acek39@gmail.com03-5363-3821

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026