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Novel Multifocal Soft Contact Lens Study

NCT06172881 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2024-05-01

Study results available
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Summary

A single site, open label protocol will be used to evaluate the safety and quality of vision of a novel soft contact lens. Habitual contact lens wearers will be asked to come to the study site for one visit. Ocular health assessments and visual acuity will be completed with both the study lens and without.

Conditions

  • Myopia

Interventions

DEVICE

Investigational Contact Lens

A soft contact lens that will be worn only at the study visit.

Sponsors & Collaborators

  • Myoptechs

    collaborator INDUSTRY

  • Ohio State University

    lead OTHER

Principal Investigators

  • Jennifer Fogt, OD, MS · The Ohio State University College of Optometry

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-12-14
Primary Completion
2024-01-12
Completion
2024-01-12
FDA Device
Yes

Countries

  • United States

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 NCT06172881 on ClinicalTrials.gov