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Clinical Evaluation of Two Multifocal Contact Lenses

NCT05457608 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 42

Last updated 2023-12-20

Study results available
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Summary

The aim of this study is to evaluate the patient subjective experiences of the monthly multifocal lens when compared to the daily disposable multifocal lens after 15 minutes of daily wear.

Conditions

Interventions

DEVICE

Lens A

monthly replacement multifocal silicone hydrogel contact lens 15 minutes of daily wear

DEVICE

Lens B

daily disposable multifocal silicone hydrogel contact lens 15 minutes of daily wear

Sponsors & Collaborators

  • CooperVision, Inc.

    lead INDUSTRY

Principal Investigators

  • Rubén V Guerrero, MSc, FIACLE · School of Optometry, National Autonomous University (UNAM)

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
42 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-06-25
Primary Completion
2022-08-13
Completion
2022-08-13
FDA Device
Yes

Countries

  • Mexico

Study Locations

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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 NCT05457608 on ClinicalTrials.gov