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Refitting Multifocal Contact Lens Wearers With a Different Multifocal Contact Lens

NCT06328660 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 66

Last updated 2025-07-28

Study results available
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Summary

The purpose of this study was to compare ease of handling and vision acuity of two multifocal contact lenses to correct presbyopia that are currently CE marked and on the UK market.

Conditions

Interventions

DEVICE

Lens 1

Frequent replacement silicone hydrogel contact lens for 14 ± 3 days on a daily disposable wearing modality

DEVICE

Lens 2

Daily disposable silicone hydrogel contact lens for 14 ± 3 days on a daily disposable wearing modality

Sponsors & Collaborators

  • CooperVision International Limited (CVIL)

    lead INDUSTRY

Principal Investigators

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SEQUENTIAL

Eligibility

Min Age
40 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-02-15
Primary Completion
2024-05-21
Completion
2024-05-21
FDA Device
Yes

Countries

  • United Kingdom

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06328660 on ClinicalTrials.gov