Eye Drop Application Monitor, Pilot Study

Status unconfirmed

Conditions studied: Cataracts, Retina Surgery, Glaucoma, Any Condition That Requires Ophthalmic Drops

In brief

The purpose of this study is to determine if an eye drop video monitoring device can accurately assess (as compared to a patient's own log or a proprietary software) the exact amount and time of eye drop delivery to a patient's eye. It is our belief that the experimental device will help patients to be more compliant by: 1) providing a viewable format so patients can see what is happening when they are applying their drops 2) providing greater accuracy to doctors regarding when and how much medication was used 3) providing greater accuracy to doctors and patients regarding how much medication was actually delivered to a patients eye.

Key facts

Study ID

NCT02639845

Run by

Alexander Eaton

People needed

500

Starts

2013-11-01

Expected to finish

2017-06-01

Last updated by the study team

2015-12-28

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Patients who are scheduled to receive prescription eye drops
• Eye drop(s) must be applied at least once a day.
• Caregivers who apply drops for patients

You may not qualify if…

• Children (patients < 18 years old)
• Those unable to self-consent

Where it is running

• Retina Health Center — Fort Myers, Florida, United States (enrolling)

Full record on ClinicalTrials.gov

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