Comparing the Performance of 1 Day Multifocal Contact Lenses

NCT04449263 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2021-06-22

Study results available
· View outcomes & findings →

Summary

The objective of the study was to compare the lens handling and performance of Lens A to habitually worn multifocal contact lenses and to the competitor Lens B.

Conditions

Interventions

DEVICE

Lens A

Subjects will be randomized to wear Lens A (test) for 2 weeks.

DEVICE

Lens B

Subjects will be randomized to wear Lens B (control) for 2 weeks.

DEVICE

Habitual Lenses

All Subjects will wear their habitual lenses for 2 weeks prior to randomization of test lens and control lens.

Sponsors & Collaborators

  • CooperVision, Inc.

    lead INDUSTRY

Principal Investigators

  • Wayne Golden · Golden Vision

  • Keith Wan · Scripps Poway Eyecare

  • Shane Kannarr · Kannarr Eye Care

  • David Ardaya · Golden Optometric Group

  • Katherine Bickle · ProCare Vision Center

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
42 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-07-27
Primary Completion
2020-12-07
Completion
2020-12-30
FDA Device
Yes

Countries

  • United States

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 NCT04449263 on ClinicalTrials.gov