Visual Performance of Center Distance Daily Disposable Multifocal Lenses

Running, not enrolling · Not applicable

Conditions studied: Myopia

In brief

The purpose of this study is to compare visual performance (high and low contrast acuity, reading acuity, contrast sensitivity, stereoacuity, accommodative response, eye hand coordination, far near vision, and dynamic vision) between Visioneering Technologies, Inc. NaturalVue Multifocal and CooperVivion MiSight.

Key facts

Study ID

NCT06475053

Run by

Visioneering Technologies, Inc

People needed

30

Starts

2024-07-31

Expected to finish

2025-12-31

Last updated by the study team

2025-09-22

Who can join

Age: 9 and older, up to 30. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Participants must satisfy the following conditions for inclusion in the trial:
• Be between 9 and 30 years of age
• Sign written Informed Consent/Assent.
• Spherical Equivalent glasses prescription: -0.50 to -7.00 diopters (D), Astigmatism: ≤ -0.75D, Anisometropia: ≤ 1.00D
• 20/20 vision in each eye
• Existing contact lens wearer
• An eye exam in last 9 months, normal stereoacuity on prior chart (or test if not available)
• No known ocular disease - anterior or posterior (posterior determined by history/chart)
• Have an acceptable or optimal fit with test lenses and be willing to wear these lenses as directed for the duration of the study.
• On examination, have ocular findings considered to be within normal limits.
• Be willing and able to follow instructions and attend the schedule of follow-up visits.

You may not qualify if…

• Any of the following will exclude a participant from this trial:
• Current hard lens wearers
• Using eye medication contraindicating lens wear such as daily use of artificial tears.
• Eye injury or surgery within twelve weeks immediately prior to enrollment for this trial.
• History of corneal refractive surgery
• Currently enrolled in an ophthalmic clinical trial that could negatively impact corneal or conjunctival health in this trial.
• Evidence of systemic or ocular abnormality, infection or disease likely to affect successful wear of contact lenses or use of their accessory solutions.
• Allergy or sensitivity to any product used in this trial.
• Pre-existing ocular condition that would contraindicate lens wear.
• Any systemic disease including autoimmune disease, immunocompromising diseases, connective tissue disease, clinically significant atopic diseases, insulin dependent diabetes, use of medications including corticosteroids and antimetabolites that may affect the eye or be exaggerated by wearing contact lenses.
• Lazy eye (Strabismus or amblyopia)
• Pupil size < 3.00 mm in either eye in dim light (measured at approximately 10 cd/m2 )

Where it is running

• The Ohio State University College of Optometry — Columbus, Ohio, United States

Full record on ClinicalTrials.gov

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