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Contrast sensitivity measurement validation testing program

Contrast sensitivity measurement validation testing program - phase 1 - test resolution determination

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN15565274
Enrollment
35
Registered
2025-07-29
Start date
2025-05-17
Completion date
Unknown
Last updated
2025-09-08

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

Conditions

Presbyopia Eye Diseases

Interventions

Part 1 will be an exploratory part following a clinic based, prospective, randomized cross-over study design testing the sensitivity to defocus of both linear sinusoidal contrast sensitivity and lette

Sponsors

Optometric Technology Group Ltd
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Age 40 to 50 years 2. Spectacle refraction: Distance: Sphere: -6.00D to + 2.00D Astigmatism: 0.00D to -0.75D Near Add +0.50 to +2.50D 3. Spectacles or soft contact lenses habitual vision correction 4. Best corrected visual acuity of at least 20/25 in each eye

Exclusion criteria

Exclusion criteria: 1. Any history of eye disease, injury or abnormality that affects any part of the eye that affects vision 2. Any active eye disease that affects any part of the eye that affects vision 3. Corneal hypoesthesia (reduced corneal sensitivity), if not aphakic 4. Newly prescribed (within the past 30 days) use of some systemic medications (such as antihistamines, decongestants, diuretics, muscle relaxants, tranquilizers, stimulants, anti-depressants, anti-psychotics, oral contraceptives) or ocular medication that may affect vision and its stability as determined by the investigator 5. Enrolment of the family members of the investigator, family members of the investigator’s staff, or individuals living in the households of these individuals

Design outcomes

Primary

MeasureTime frame
Measurement of Contrast sensitivity at photopic (85cd/m²) and mesopic (3cd/m²) luminance using timed controlled contrast sensitivity visual acuity with the OTGi vision suite and M&S Technology between four and nine times during the study visit

Secondary

MeasureTime frame
Measurement of high contrast timed logMAR visual acuity at photopic (85 cd/m²) luminance using timed controlled visual acuity using OTGi vision suite 9 times during the first study visit

Countries

England, United Kingdom

Contacts

Public ContactDeborah Moore
dmoore@otg.co.uk+44 2072224224

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026