Clinical Investigation of the Vision-R800 Device.

Completed · Phase 4

Conditions studied: Myopia, Hyperopia, Astigmatism, Presbyopia

In brief

Randomized, bilateral, cross-over dispensing study of a standard and VR800 refraction and associated spectacle lenses.

Key facts

Study ID

NCT04208750

Run by

Pete Kollbaum, OD, PhD

People needed

119

Starts

2019-11-18

Expected to finish

2021-02-01

Last updated by the study team

2022-03-14

Who can join

Age: 18 and older, up to 70. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• current adaptated progressive addition lens wearer, if bifocal lens required
• wearable pair of glasses < 2 years old
• wear glasses at least 6 hours per day

You may not qualify if…

• Eye Disease with an impact on visual acuity or binocular vision abnormalities (by self-report)
• Formal training in optometry, vision science or in the eyecare field

Where it is running

• Indiana University Clinical Optics Research Lab — Bloomington, Indiana, United States

Full record on ClinicalTrials.gov

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