Evaluation of Visual Performance With Contact Lenses

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

26 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-06-14

Study Completion Date

2018-07-26

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This study will evaluate the influence of contact lens optical design on visual performance using standard and multifocal soft contact lenses (MFCLs).

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Visual Outcomes for Toric Efficacy Study

NCT03728218

Astigmatism Myopia

COMPLETED NA

Evaluating Contact Lens Optics

NCT05028790

Myopia

COMPLETED NA

Novel Multifocal Soft Contact Lens Study

NCT06172881

Myopia

COMPLETED NA

Contact Lens Optics and Visual Performance

NCT05308069

Myopia

COMPLETED NA

A Clinical Evaluation of Two Contact Lenses Used With Three Care Systems

NCT04195581

Myopia

COMPLETED NA

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

The study will examine visual acuity with various contact lenses, with and without glare source, in myopes between the ages of 18-39 years old (inclusive) to determine the effect of different multifocal optical designs on visual performance in the post-fit period.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Myopia

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Group 1

All subjects will wear the 3 contact lenses: Single Vision, Multifocal 1 and Multifocal 2.

Single Vision Contact Lens

Intervention Type DEVICE

Spherical Contact Lens worn on non-dispensing basis

Multifocal Contact Lens 1

Intervention Type DEVICE

Multifocal Contact Lens worn on non-dispensing basis

Multifocal Contact Lens 2

Intervention Type DEVICE

Multifocal Contact Lens worn on non-dispensing basis

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Single Vision Contact Lens

Spherical Contact Lens worn on non-dispensing basis

Intervention Type DEVICE

Multifocal Contact Lens 1

Multifocal Contact Lens worn on non-dispensing basis

Intervention Type DEVICE

Multifocal Contact Lens 2

Multifocal Contact Lens worn on non-dispensing basis

Intervention Type DEVICE

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

comfilcon A comfilcon A etafilcon A

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* 18 to 39 years of age
* Best corrected visual acuity of at least 20/30
* Spherical equivalent refractive error in each eye of between -0.75 and -6.00 diopters sphere after vertexing to the corneal plane

Exclusion Criteria

* Greater than -1.00 diopter of refractive astigmatism at the corneal plane
* Any active anterior segment disease, pathology, or surgery affecting vision, refraction, or the ability to wear a soft contact lens
* History of ocular trauma or surgery causing abnormal or distorted vision
* Current Rigid Gas Permeable (RGP) contact lens wearers
* Unwilling to have eyes photographed or video recorded
* Pregnant and/or lactating females, by self-report

Minimum Eligible Age

18 Years

Maximum Eligible Age

39 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes