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Evaluation of enophthalmos due to ophthalmic solution for glaucoma

Evaluation of enophthalmos due to ophthalmic solution for glaucoma - Enophthalmos due to ophthalmic solution for glaucoma

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000018596
Enrollment
15
Registered
2015-08-07
Start date
2015-08-07
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

Glaucoma

Interventions

None listed

Sponsors

Department of Ophthalmology, Shiga University of Medical Science
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Outpatients of Shiga University of Medical Science Hospital that start the treatment with bimatoprost ophthalmic solution for glaucoma

Exclusion criteria

Exclusion criteria: Patients who have the history of the treatment with prostaglandin ophthalmic solution Patients who can not undergo MRI examination

Design outcomes

Primary

MeasureTime frame
Variation on a value of proptosis

Secondary

MeasureTime frame
Variation on a volume of orbital fatty tissue

Countries

Japan

Contacts

Public ContactTomoaki Higashiyama

Shiga University of Medical Science Department of Ophthalmology

higashi@belle.shiga-med.ac.jp0775482276

Outcome results

None listed

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