ClinConnect ClinConnect Logo
Search / Trial NCT02871817

A Comparison of the Checkup Vision Assessment System to Standard Vision Assessment Tools

Launched by DIGISIGHT TECHNOLOGIES, INC. · Aug 15, 2016

Trial Information

Current as of September 06, 2025

Unknown status

Keywords

Near Corrected Visual Acuity Early Treatment Diabetes Retinopathy Study Amsler Grid Home Monitoring

ClinConnect Summary

BACKGROUND AND INTRODUCTION Neovascular Age - related Macular Degeneration (AMD) is the most common cause of vision loss in subjects over the age of 60. Today in the US over 15 million people live with some form of AMD, and approximately 1.6-1.75 million people have neovascular AMD associated with vision loss. Approximately 200,000 new cases are diagnosed in the US annually; worldwide, approximately 500,000 new cases are diagnosed each year. With the aging of the overall population, prevalence of all forms of AMD is expected to rise to as many as 42 million by 2030, and it is projected that...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Male or female 18 years of age and older
  • Best Corrected Near Visual acuity 20/200 or better in study eye(s)
  • Able and willing to make the required study visits
  • Able and willing to provide consent and comply with study assessments for the full duration of the study.
  • Specific Inclusion Criteria for Subgroup with Normal Eyes
  • Best Corrected Near Visual acuity 20/32 or better in each eye
  • No concurrent systemic illness affecting the retina and vision.
  • Specific Inclusion Criteria for Subgroups with AMD or DR
  • Diagnosis of either AMD or DR (all subgroups qualify)
  • Exclusion Criteria:
  • Dementia or other neurologic or psychological limitation that would prevent the patient from performing regular self-testing of visual function
  • Other comorbid ocular pathology affecting vision (with the exception of cataract, pseudophakia, refractive error, and/or presbyopia)
  • Inability to successfully undergo training and certify ability to self-test with Paxos Checkup
  • Inability to return for follow up

About Digisight Technologies, Inc.

Digisight Technologies, Inc. is a pioneering clinical trial sponsor specializing in the development of innovative digital solutions for healthcare and clinical research. With a focus on leveraging cutting-edge technology, the company aims to enhance patient engagement, streamline data collection, and improve the overall efficiency of clinical trials. Committed to advancing medical knowledge and patient outcomes, Digisight collaborates with healthcare providers, researchers, and regulatory bodies to facilitate the successful execution of trials that address critical health challenges. Their expertise in digital health tools positions them as a leader in transforming the landscape of clinical research.

Locations

San Antonio, Texas, United States

Miami, Florida, United States

Cleveland, Ohio, United States

Phoenix, Arizona, United States

Lexington, Kentucky, United States

Reno, Nevada, United States

Austin, Texas, United States

Spokane, Washington, United States

Tallahassee, Florida, United States

Fort Myers, Florida, United States

Mountain View, California, United States

Nashville, Tennessee, United States

Patients applied

0 patients applied

Trial Officials

Carol Hoang

Study Director

Digisight Technologies, Inc.

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Similar Trials