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Questionnaire survey on the usability of eye drop aid Just in in patients with glaucoma

Questionnaire survey on the usability of eye drop aid Just in in patients with glaucoma - Questionnaire survey on the usability of eye drop aid

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000040646
Enrollment
70
Registered
2020-08-01
Start date
2020-08-01
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

Glaucoma

Interventions

None listed

Sponsors

Kobe University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Glaucoma patients visiting the ophthalmology department of Kobe University Hospital. Self-instillation

Exclusion criteria

Exclusion criteria: Those with best corrected visual acuity less than 0.1 for both eyes Those who had undergone intraocular surgeries within 1 month (for glaucoma filtrating surgeries, within three months).

Design outcomes

Primary

MeasureTime frame
Usability of Just in

Countries

Japan

Contacts

Public ContactYasutaka Takagi

Santen Pharmaceutical Co., Ltd. Japan Medical Affairs

clinical@santen.co.jp06-4802-9603

Outcome results

None listed

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