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Completed Not applicable Interventional Accepts healthy volunteers Results available

eSight Eyewear Quality of Life and Efficacy Study

ClinicalTrials.gov ID: NCT02616900

Public ClinicalTrials.gov record NCT02616900. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 6, 2026, 5:13 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

eQUEST -- ESIGHT QUALITY OF LIFE AND EFFICACY STUDY A Multi-center, Prospective Cohort Study to Assess the Impact of eSight Eyewear on Functional Vision Improvement and Quality of Life in a Low Vision Population

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The "eSight Quality of Life and Efficacy Study" (eQUEST) is a prospective cohort study intended to demonstrate the functional vision and Quality of Life (QoL) improvement provided by eSight Eyewear to persons with significant visual impairment resulting from various eye conditions. The multi-site study will evaluate the efficacy of the eSight device for various Activities of Daily Living (ADLs) across a broad range of subject ages and disease types.

Study identification

NCT ID
NCT02616900
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
eSight Corporation
Industry
Enrollment
74 participants

Conditions and interventions

Conditions

Interventions

Device

Eligibility (public fields only)

Age range
13 Years to 75 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 15, 2015
Primary completion
Mar 30, 2017
Completion
Mar 30, 2017
Last update posted
Apr 4, 2019

2015 – 2017

United States locations

U.S. sites
4
U.S. states
3
U.S. cities
4
Facility City State ZIP Site status
Vitreous and Retina Consultants PA Lakeland Florida 33805
Lighthouse For the Blind of the Palm Beaches West Palm Beach Florida 33407
Johns Hopkins University School of Medicine, Wilmer Eye Institute Baltimore Maryland 21903
University of Michigan Kellogg Eye Center Ann Arbor Michigan 48105

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02616900, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 4, 2019 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02616900 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →