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Performance evaluation research of Tear Film measurement device

Performance evaluation research of Tear Film measurement device in MGD and Dry Eye patients.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1080225054
Enrollment
50
Registered
2020-02-06
Start date
2020-02-06
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

MGD and dry eye

Interventions

investigational material(s) Generic name etc : Tear Film measurement device INN of investigational material : - Therapeutic category code : Dosage and Administration for Investigational material : In

Sponsors

Santen pharmaceutical co.,ltd
Lead Sponsor
Clinical Operations Japan/ASIA Group
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: For MGD patients group - Diagnosed as hyposecretory MGD For dry eye patients group - Diagnosed as aqueous tear deficiency dry eye For Non-MGD and Non-dry eye patients group - Diagnosed not as hyposecretory MGD and aqueous tear deficiency dry eye

Exclusion criteria

Exclusion criteria: - Active disease such as eye trauma or corneal infection - Punctal Plug

Design outcomes

Primary

MeasureTime frame
exploratory Value of tear film assessment

Secondary

MeasureTime frame
exploratory BUT

Countries

Japan

Outcome results

None listed

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