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Evaluation of The Clinical Acceptance of Soft Contact Lenses for Myopia Control

NCT04709237 · Status: COMPLETED · Type: INTERVENTIONAL · Enrollment: 21

Last updated 2024-08-27

Study results available
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Summary

The main objective of the study was to evaluate the clinical acceptance of soft contact lenses for Myopia control.

Conditions

  • Myopia

Interventions

DEVICE

omafilcon A control lens

Participants were randomized to wear omafilcon A control soft contact lens for 10 days.

DEVICE

omafilcon A test lens 1

Participants were randomized to wear omafilcon A test soft contact lens 1 for 10 days.

DEVICE

omafilcon A test lens 2

Participants were randomized to wear omafilcon A test soft contact lens 2 for 10 days.

Sponsors & Collaborators

  • CooperVision, Inc.

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
10 Years
Max Age
16 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-12-14
Primary Completion
2021-03-31
Completion
2021-03-31

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 NCT04709237 on ClinicalTrials.gov