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Treatment efficacy of 0.05% cyclosporine eyedrop on ocular surface changes after anti-glaucoma medication in glaucoma patients.

Treatment efficacy of 0.05% cyclosporine eyedrop on ocular surface changes after anti-glaucoma medication in glaucoma patients.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0007124
Enrollment
30
Registered
2022-03-28
Start date
2020-09-24
Completion date
Unknown
Last updated
2022-04-04

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

Conditions

None listed

Interventions

None listed

Sponsors

Keimyung University Dongsan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) A patient with glaucoma who is 19 years of age or older and has been instilling one or more antiglaucoma eye drops bilaterally for at least one, 2) Based on the Korean dry eye treatment guidelines at the time of first enrolling, and the diagnostic criteria presented by the Dry Eye Workshop in 2007, dry eye syndrome of level 2 or higher 3) Patients who can be followed up for at least 4 months 4) Patients who accurately understands the details of the clinical trial and has written a consent form from a voluntary doctor

Exclusion criteria

Exclusion criteria: 1) Level 1 and 2 mild dry eye syndrome patients 2) Those who have had hypersensitivity reactions to this drug or other drugs, or those with a history of clinically significant hypersensitivity reactions 3) Patients who are pregnant, lactating, or planning to become pregnant 4) Those who participated in other clinical trials within 3 months before the first administration date 5) If there is a history of corneal or glaucoma surgery or intraocular surgery within 6 months of screening 6) Patients who want to wear contact lenses during the clinical trial period 7) Patients with eye diseases that require treatment other than dry eye syndrome and glaucoma 8) Patients received lacrimal punctal surgery (punctal plug and surgical lacrimal closure) within 1 month before instillation

Design outcomes

Primary

MeasureTime frame
Ocular surface disease index;Tear break up time;Ocular surface score

Secondary

MeasureTime frame
Best corrected visual acuity;intraocular pressure;tear meniscus height;Matrix metalloproteinase-9;tear osmolality;Schirmer's test;Visual field test

Countries

Korea, Republic of

Contacts

Public ContactJong Hwa Jun

Keimyung University Dongsan Hospital

junjonghwa@gmail.com+82-53-258-4555

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 9, 2026