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Evaluation of safety and efficacy of gonioscope "GS-1"(NIDEK)

Evaluation of safety and efficacy of gonioscope "GS-1"(NIDEK) - Evaluation of safety and efficacy of GS-1

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000036831
Enrollment
100
Registered
2019-05-23
Start date
2019-05-23
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

Chukyo Eye Clinic
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Case which gonioscopy by gonioscope and GS-1 be conducted at Chukyo Eye Clinic

Exclusion criteria

Exclusion criteria: Case without consent from the subject

Design outcomes

Primary

MeasureTime frame
1.Required time for gonioscopy by gonioscope and GS-1 2.Comparison of discomfort and pain caused by gonioscope and GS-1 3.Accuracy of gonioscopy by GS-1 compared to gonioscope 4.Comparison of angle evaluation by GS-1 and anterior OCT 5.Evaluation of distinctive angle observation in outflow reconstruction response and resistant example

Countries

Japan

Contacts

Public ContactMitsunori Watanabe

Chukyo Eye Clinic Chukyo Eye Clinic

watanabe@chukyogroup.jp052-883-1543

Outcome results

None listed

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