A randomized study comparing topical rebamipide with artificial tears in the treatment of dry eye with contact lens wearers

A randomized study comparing topical rebamipide with artificial tears in the treatment of dry eye with contact lens wearers - A randomized study comparing topical rebamipide with artificial tears in the treatment of dry eye with contact lens wearers

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000011397

Enrollment

Registered

2013-08-07

Start date

2013-08-10

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

dry eye

Interventions

rebamipide ophthalmic suspension artificial tears

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: dry eye patients soft contact lens wearers

Exclusion criteria

Exclusion criteria: People with anterior segment eye diseases except dry eye disease Patients with severe posterior segment eye diseases Patients who use steroid, anti-inflammatory and immune suppression drugs Patients who take any anti-oxidant supplements. Patients with serious systemic diseases Patients who had any ocular surgery within 12 month prior to signing the informed consent Patients who had any punctual occlusion within 1 month prior to signing the informed consent People whom the investigator or the subinvestigators consider to be ineligible for the intervention therapy in any other reason

Design outcomes

Primary

Measure	Time frame
dry eye parameters (subjective and objective findings)	—

Countries

Japan

Contacts

Public ContactMotoko Kawashima

Keio University School of Medicine Ophthalmology

motoko326@gmail.com0353633866

Outcome results

None listed

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