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NCT05325996

Evaluating Home Testing Devices for the Management of Glaucoma

Completed NA Last updated 14 November 2025
What this trial tests

NA trial testing Standard Automatic Perimetry Humphrey Field Analyzer in Glaucoma, Open-Angle in 53 participants. Completed in 17 February 2025.

Timeline
15 April 2022
Primary endpoint
17 February 2025
17 February 2025

Quick facts

Lead sponsorWills Eye
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposediagnostic
Enrollment53
Start date15 April 2022
Primary completion17 February 2025
Estimated completion17 February 2025
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Wills Eye — full company profile →

Who can join

Adults 20 to 80, any sex, with Glaucoma, Open-Angle. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

With the advancement in technology we have the opportunity of performing the glaucoma testing at home to monitor the disease. The purpose of this study is evaluating the feasibility and patient acceptance of home testing with head mounted perimetry; detection of progression with head mounted perimetry vs office based perimetry; and monitoring the eye pressure measured by patients at home using a portable tonometer.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of Standard Automatic Perimetry Humphrey Field Analyzer

Trials testing the same drug.

Other recruiting trials for Glaucoma, Open-Angle

Currently open trials in the same condition.

Other Wills Eye trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05325996.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing