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Clinical Comparison of Two Soft Contact Lenses

NCT06251154 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2024-08-22

Study results available
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Summary

This study was designed to gather short-term clinical performance data for 2 soft contact lenses.

Conditions

  • Myopia

Interventions

DEVICE

Lens 1

Daily disposable silicone hydrogel contact lens (diameter=14.0mm) for 15 minutes

DEVICE

Lens 2

Daily disposable silicone hydrogel contact lens (diameter=14.1mm) for 15 minutes

Sponsors & Collaborators

  • CooperVision, Inc.

    lead INDUSTRY

Principal Investigators

  • Carole Maldonado-Codina, PhD MCOptom · Eurolens Research

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-12-11
Primary Completion
2024-01-08
Completion
2024-01-08
FDA Device
Yes

Countries

  • 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 NCT06251154 on ClinicalTrials.gov