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Effect of multifocal contact lenses on binocular vision

Quantification of binocular summation of multifocal and monovision contact lenses

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN13386434
Enrollment
30
Registered
2021-10-18
Start date
2021-10-18
Completion date
Unknown
Last updated
2022-04-25

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

Conditions

Presbyopia Eye Diseases Presbyopia

Interventions

In this study the researchers will measure the visual performance and binocular performance of various control multifocal contact lenses compared to a test multifocal contact lens, and a control mono

Sponsors

CooperVision International Limited
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. 40 or more years of age 2. Have read and understood the Participant Information Sheet in English 3. Have read, signed and dated the Informed Consent 4. Current multifocal contact lens wearer 5. Spectacle refraction: Distance: Sphere: -6.00D to + 4.00DS Astigmatism: -0.00DC to -0.75DC in each eye Near Addition: +0.75D to +2.50D 6. Best corrected visual acuity of at least 20/25 in each eye 7. Have normal eyes with the exception of the need for visual correction 8. Be willing and able to adhere to the instructions set in the clinical protocol and maintain the appointment schedule

Exclusion criteria

Exclusion criteria: 1. Ocular anterior segment infection, inflammation, abnormality, or active disease that would contraindicate contact lens wear 2. Use of systemic or ocular medications for which contact lens wear could be contraindicated as determined by the investigator 3. Monocular participants (only one eye with functional vision) or participants fit with only one lens 4. Any moderate or severe ocular condition observed during the slit lamp examination at the enrolment visit 5. History of herpetic keratitis, ocular surgery or irregular cornea 6. Known pregnancy or lactation during the study period 7. Enrolment of the investigator or his/her staff, 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
1. Overall binocular timed visual acuity measured in logMAR after approximately 30 minutes of contact lens wear 2. Overall monocular timed visual acuity measured in logMAR after approximately 30 minutes of contact lens wear 3. Binocular vision measured in arcseconds after approximately 1 hour of contact lens wear

Secondary

MeasureTime frame
There are no secondary outcome measures

Countries

England, United Kingdom

Contacts

Public ContactDeborah Moore
dmoore@otg.co.uk+44 (0)207 2224224

Outcome results

None listed

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