Novel Multifocal Soft Contact Lens Study

Completed · Not applicable

Conditions studied: Myopia

In brief

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.

Key facts

Study ID

NCT06172881

Run by

Ohio State University

People needed

10

Starts

2023-12-14

Expected to finish

2024-01-12

Last updated by the study team

2024-05-01

Who can join

Age: 18 and older, up to 40. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Ability to give informed consent
• Any gender
• Any racial or ethnic origin
• 18 - 40 years of age
• Distance visual acuity with best corrected visual acuity of 20/25 with each eye
• Habitual soft contact lens wearer with myopia
• Good general health (defined by medication use that has not changed within the last month and the absence of medical conditions or treatments that are deemed confounding to the data as determined by the investigator).

You may not qualify if…

• Current or active ocular inflammation or infection as determined by the Investigator.
• Astigmatism > 0.75 D in either eye
• History of previous eye surgery
• Demonstration or history of corneal ectasia or keratoconus.
• Pregnant or lactating.

Where it is running

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

Full record on ClinicalTrials.gov

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