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Evaluation of efficacy of diquafosol sodium eyedrop

Evaluation of efficacy of diquafosol sodium eyedrop - Evaluation of efficacy of diquafosol sodium eyedrop

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000018510
Enrollment
30
Registered
2015-08-01
Start date
2015-06-22
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

Meibomian gland dysfunction

Interventions

Sponsors

Inouye Eye Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Over 20years old 2. Male and Female 3. Patients diagnosed as dry eye 4. Patients with MGD

Exclusion criteria

Exclusion criteria: 1. atients who use dry eye or MGD treatment within 2 weeks before a study starts. 2. Patient who have a previous history of treatment intended to become obstructed lacrimal puncta. 3. Patients who need to use eyedrops other than test drugs during a study. 4. Patients who have anatomically and functionally abnormal eyelid. 5. Patients with surgical history in the internal eye (including laser therapy) within 3 months prior to initiation of the clinical research. 6. Patients who have a previous allergy to drugs that they use during a study. 7. Patients who have any other reasons that causes the study doctor to deem a subject unsuitable for the study

Design outcomes

Primary

MeasureTime frame
1. Symptoms 2. Slit lamp 3. Tear film breakup time 4. Meibography 5.Tear volume , Tear thickness

Countries

Japan

Contacts

Public ContactShiro Amano

Inouye Eye Hospital Ophthalmology

amanoshiro1126@gmail.com03-3295-0911

Outcome results

None listed

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