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Eye Drop Application Monitor, Pilot Study

NCT02639845 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 500

Last updated 2015-12-28

No results posted yet for this study

Summary

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.

Conditions

  • Cataracts
  • Retina Surgery
  • Glaucoma
  • Any Condition That Requires Ophthalmic Drops

Sponsors & Collaborators

  • California Retina Consultants

    collaborator OTHER

  • Konowal Vision Center

    collaborator UNKNOWN

  • Southwest Florida Eye Care

    collaborator UNKNOWN

  • Alexander Eaton

    lead INDUSTRY

Principal Investigators

  • Soratree Charoenthongtrakul, Ph.D. · Retina Health Center

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2013-11-30
Primary Completion
2016-12-31
Completion
2017-06-30

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02639845 on ClinicalTrials.gov