Exploratory study for dry eye patient satisfaction with treatment

Exploratory study for dry eye patient satisfaction with treatment - Exploratory study for dry eye patient satisfaction with treatment

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000030038

Enrollment

100

Registered

2017-11-20

Start date

2017-11-10

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

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 20 years of age or over Regardless of sex Diagnosed dry eye and use Diquafosol sodium ophthalmic solution or Sodium hyaluronate ophthalmic solution 0.1% for more than 3 months.

Exclusion criteria

Exclusion criteria: Having advanced ocular disorder due to ocular pemphigus or Stevens Johnson syndrome Using a punctal plug and performing a punctal closure procedure Diquafosol sodium ophthalmic solution and sodium hyaluronate ophthalmic solution are used in combination. Treated with Rebamipide suspension eye drop Subject with hypersensitivity to fluorescein The investigator judges that the subject is ineligible as the study subject.

Design outcomes

Primary

Measure	Time frame
Treatment satisfaction Factor analysis of satisfaction Relationship between patient background and ophthalmic findings / symptoms	—

Countries

Japan

Contacts

Public ContactKazuhisa Suwaki

Santen Pharmaceutical Co., Ltd. FOTE Team

clinical@santen.co.jp06-4802-9604

Outcome results