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Measuring Changes In Choroidal Thickness Induced By Prototype Soft Contact Lenses Worn For 1 Hour

NCT07155551 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2025-09-04

No results posted yet for this study

Summary

The objective of the study is to evaluate the short-term change in choroidal thickness induced by 3 prototype soft contact lenses for people with myopia.

Conditions

  • Myopia; Refractive Error

Interventions

DEVICE

Lens A

Lens A of Study P/883/24/MO

DEVICE

Lens B

Lens B of Study P/883/24/MO

DEVICE

Lens C

Lens C of Study P/883/24/MO

Sponsors & Collaborators

  • University of Waterloo School of Optometry and Vision Science

    collaborator UNKNOWN

  • Myoptechs, Inc

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
DOUBLE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
25 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-08-25
Primary Completion
2025-12-31
Completion
2025-12-31
FDA Device
Yes

Countries

  • Canada

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 NCT07155551 on ClinicalTrials.gov