MedTrace Logo

Comparing The Performance Of Two Different Daily Disposable Lenses (MIKI)

NCT04492397 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 35

Last updated 2021-06-23

Study results available
· View outcomes & findings →

Summary

The objective of the study is to evaluate and compare the performance of study test lens to study control lens, when worn on a daily disposable modality over a period of approximately one week each

Conditions

  • Myopia

Interventions

DEVICE

Test Contact Lens

Subjects will be randomized to wear test lenses.

DEVICE

Control Contact Lens

Subjects will be randomized to wear control lenses.

Sponsors & Collaborators

  • CooperVision, Inc.

    lead INDUSTRY

Principal Investigators

  • Lyndon Jones, PhD FCOptom · University of Waterloo

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
17 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-09-30
Primary Completion
2021-03-31
Completion
2021-03-31
FDA Device
Yes

Countries

  • Canada

Study Locations

More Related Trials

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 NCT04492397 on ClinicalTrials.gov