Comparison of Adherence Between Diquas LX3% Eye Drops and Diquas 3% Eye Drops: A Prospective Randomized Non-Blind Intervention Study

Comparison of Adherence Between Diquas LX3% Eye Drops and Diquas 3% Eye Drops: A Prospective Randomized Non-Blind Intervention Study - Comparison of Adherence Between Diquas LX3% Eye Drops and Diquas 3% Eye Drops

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000052920

Enrollment

120

Registered

2023-11-27

Start date

2024-02-01

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 disease

Interventions

Diquas LX Eye Drops 3% group Diquas Eye Drops 3% group

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Individuals who understand and consent to the consent form. 2. Individuals aged 20 years and older.

Exclusion criteria

Exclusion criteria: 1. Individuals deemed unsuitable as study participants by the principal investigator. 2. Individuals from whom consent could not be obtained.

Design outcomes

Primary

Measure	Time frame
Adherence	—

Secondary

Measure	Time frame
Dry eye treatment efficacy	—

Countries

Japan

Contacts

Public ContactTakenori Inomata

Juntendo University Graduate School of Medicine, Department of Ophthalmology

tinoma@juntendo.ac.jp03-3813-3111

Outcome results

None listed

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