Comparative Study comparing the Clinical Efficacy and Patients Satisfaction of Preservative and Preservative-free Diquafosol 3% Eye Drops in Dry Eye Patients

Prospective, Single Center Comparative Study comparing the Clinical Efficacy and Patients Satisfaction of Preservative and Preservative-free Diquafosol 3% Eye Drops in Dry Eye Patients

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0002585

Enrollment

Registered

2017-12-06

Start date

2017-09-13

Completion date

Unknown

Last updated

2019-03-11

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

Conditions

None listed

Interventions

Drug : The intervention group is different depending on which eye drops are used first among Diquas and Diquas-s eye drop (6 times a day).

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: - Patients who had been diagnosed with dry eye syndrome at the Korea University Ansan Hospital between the IRB approval date and May 30, 2018. - Dry eye syndrome with symptoms of at least 3 months - Tear film break-up time is less than 5 seconds - The corneal staining grade is 1 or more

Exclusion criteria

Exclusion criteria: - Eyes with previous ocular damage or active eye infection - Patients with non-dry eye inflammation - If there is ophthalmologic surgery or trauma history within the last 6 months - Under 19 years of age

Design outcomes

Primary

Measure	Time frame
Adverse reactions;Paient satisfaction	—

Secondary

Measure	Time frame
Ocular surface disease index (OSDI) score;Fluorescein sodium corneal staining grade;Tear break-up time (TBUT);Schirmer test	—

Countries

Korea, Republic of

Contacts

Public ContactYoungsub Eom

Korea University Ansan Hospital

hippotate@hanmail.net+82-2-925-0532

Outcome results