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Comparing Silicone Hydrogel Contact Lens Wearers to Hydrogel Contact Lens Wearers and Non-lens Wearers

NCT04886479 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 22

Last updated 2024-01-30

Study results available
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Summary

This study was a multi-site, prospective, randomized, non-masked, unilateral, non-dispensing study.

Conditions

  • Myopia

Interventions

OTHER

Control

No lens

DEVICE

Test Lens

Low Dk HEMA contact lens worn for 3 hours

Sponsors & Collaborators

  • CooperVision, Inc.

    lead INDUSTRY

Principal Investigators

  • Lyndon Jones, PhD FCOptom · Centre for Ocular Research & Education

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
17 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-03-06
Primary Completion
2022-10-07
Completion
2022-10-07
FDA Device
Yes

Countries

  • Canada
  • United Kingdom

Study Locations

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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 NCT04886479 on ClinicalTrials.gov