dacryocystitis
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients who meet all of the following criteria are included in this study. 1) Male or female 2) Inpatients or ambulatory patients 3) Patients who are aged of 20 years or older when giving their consent 4) Patients who completed treatment of dacryocystitis accompanied with lacrimal sac calculi
Exclusion criteria
Exclusion criteria: Patients who fall into any of the following criteria are excluded from participating in the study. 1) Patients whose history of rebamipide ophthalmic solution use is unknown (within 2 years after onsent of main symptom caused by the dacryocystitis accompanied with lacrimal sac calculi in the eye to be investigated)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Gender Age, Birthdate Eye to be investigated The day of onset and type of dacryocystitis-related symptoms in the eye to be investigated (lacrimation, eye discharge, swelling, feeling of calculus, and others) Treatment, course, and outcome of lacrimal sac calculi in the eye to be investigated Use of rebamipide ophthalmic solution Medication (name of drug, purpose of use, usage and dose, date of the initial administration, date of completion of the administration) History of punctal plug use Complications (on eyes or systemic) History of lacrimal duct obstruction or dacryocystitis, period, and treatment Habit of smoking, daily number of cigarettes, years of smoking history Habit of alcohol drinking, type of alcohol, average daily intake Composition of lacrimal sac calculi in the eye to be investigated (rebamipide, protein, borate, and calcium phosphate) Bacterial culture and identification Dacryocystography Schirmer's test Corneal fluorescein staining DEQS (Dry Eye related Quality of life Score) | — |
Countries
Japan
Contacts
Soiken, Inc. Clinical Study Support Division