Subjects who would benefit from undergoing lid hygiene therapy or normal subjects
Conditions
Interventions
Safety and efficacy are verified at the Ophthalmology Department by performing estimations before and after wiping lid margins using tap-water alone.
Safety and efficacy are verified at the Ophthalmol
Sponsors
Department of Ophthalmology, Ashikaga Red Cross Hospital
Department of Ophthalmology, Keio University School of Medicine (Tokyo), Ishida Eye Clinic (Shizuoka), Wada Eye Clinic (Chiba)
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Subjects who agree to the ophthalmological examinations
Exclusion criteria
Exclusion criteria: Subjects who are judged to have poor understanding or who are unlikely to perform the required tasks of the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| subjective symptom, tear breakup time, fluorescein staining score, meibum, lid margin findings, other related items. Evaluations are conducted at the starting point and at 2 and 3 months. | — |
Countries
Japan
Contacts
Public ContactHirotaka Tanabe
Ashikaga Red Cross Hospital Ophthalmology
Outcome results
None listed