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Investigating methods of measuring visual field sensitivity in glaucoma

Novel perimetry for identifying changes in visual field sensitivity in glaucoma

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN88711666
Enrollment
387
Registered
2023-04-21
Start date
2022-08-01
Completion date
Unknown
Last updated
2026-08-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Investigating peripheral visual sensitivity in people with glaucoma and normally-sighted individuals Eye Diseases Glaucoma

Interventions

1. Eligibility screening tests: 1.1. Questions about eye and general health history, family history, and current medications 1.2. Measurement of vision on a standard eye chart 1.3. Measurement of eye

Sponsors

Cardiff University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 120 Years

Inclusion criteria

Inclusion criteria: Patients with glaucoma: 1. Diagnosis of Primary Open Angle Glaucoma (POAG) or Normal Tension Glaucoma (NTG) by the hospital eye service 2. Visual field defect consistent with glaucomatous optic nerve appearance. 3. Stable IOP <21 mmHg 4. Refractive error < ±6.00DS and <3.50DC 5. Visual acuity of 6/9 (+0.3 logMAR) or better in the test eye, in the absence of significant corneal or media opacities 6. Age over 40 years Normally-sighted individuals: 1. No clinical diagnosis of glaucoma or other retinal disease 2. Full visual field 3. Healthy optic disc 4. No family history of glaucoma (first-degree) 5. Refractive error <±6.00DS and <3.50DC 6. Visual acuity of 6/9 (+0.3 logMAR) or better in the test eye, in the absence of significant corneal or media opacities 7. Age over 40 years

Exclusion criteria

Exclusion criteria: 1. Any systemic disease and/or medication which is likely to affect visual performance (e.g. diabetes, thyroid disease) 2. Any ocular disease and/or medication that may affect visual performance (apart from glaucoma) 3. Any previous ocular surgery which may degrade visual performance (e.g. corneal graft, photodynamic therapy) 4. Inability to steadily fixate during the test (e.g. individuals who have nystagmus or macular degeneration)

Design outcomes

Primary

MeasureTime frame
The difference in visual sensitivity between patients and normally-sighted individuals is measured at months 11, 22, and 39

Secondary

MeasureTime frame
Variance of visual sensitivity in patients and normally-sighted individuals is measured at months 11, 22, and 39

Countries

England, Northern Ireland, United Kingdom, Wales

Contacts

Public ContactBecky Vangasse
vangasser@cardiff.ac.uk+ 44 (0)2920870564

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Aug 25, 2026