MedTrace Logo

Evaluating Two Multifocal Daily Disposable Contact Lenses

NCT05579886 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2024-02-20

Study results available
· View outcomes & findings →

Summary

The objective of the study was to adapt existing multifocal soft lens wearers to a Control Lens for at least 2 weeks and then evaluate the success of switching them to the Test Lens, with a review after 2 weeks.

Conditions

Interventions

DEVICE

Control Lens

Daily disposable multifocal soft lens with 2 add design (2ADD) for 2 weeks

DEVICE

Test Lens

Daily disposable multifocal soft lens with 3 add design (3ADD) for 2 weeks

Sponsors & Collaborators

  • Centre for Ocular Research & Education, Canada

    collaborator OTHER

  • CooperVision, Inc.

    lead INDUSTRY

Principal Investigators

  • Andrew Sacco · Sacco Eye Group

  • Shane Kannarr · Kannarr Eye Care

  • Katherine Bickle · ProCare Vision Center

  • Michael Cymbor · Nittany Eye Associates

  • Roxanne Achong-Coan · Coan Eye Care & Optical Boutique

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
42 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-10-10
Primary Completion
2023-02-07
Completion
2023-02-07
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 NCT05579886 on ClinicalTrials.gov