Clinical trial Recruiting at 1 site Interventional Ages 18 to 99

World Sight Foundation Field Machine pilot in glaucoma care

Official title: Clinical Testing Pilot of the World Sight Foundation Field Machine (WSFFM) in Glaucoma Patients - Comparison With Humphrey Visual Field Analyser

Run by Buckinghamshire Healthcare NHS Trust · NCT07674069 · Data updated 2026-11-12

This pilot tests a new field machine to see if it can help identify moderate to severe glaucoma in patients at a eye clinic, compared with the standard Humphrey Visual Field test.

Quick facts

Study typeInterventional
Ages18 Years to 99 Years
SexAll
Enrollment100 (estimated)
SponsorBuckinghamshire Healthcare NHS Trust
Academic / other
Locations1 site (Aylesbury)
StatusRecruiting
StartedApril 29, 2026
Main results expectedJuly 1, 2026
Study endsJuly 1, 2026
Registry record updatedJune 29, 2026
Trial IDNCT07674069 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults 18 years or older attending a glaucoma outpatient clinic who require visual field testing using HVF standard protocols.

Probably not a fit

Patients who do not require visual field testing during their visit or who are unable to perform the test may derive no direct benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This exploratory pilot study evaluates how well the World Sight Foundation Field Machine performs in identifying moderate to severe visual field loss among glaucoma patients at a single NHS clinic. It compares WSFFM to the gold-standard HVF analyser, acknowledging it is not expected to be equivalent or non-inferior, but to provide insight into the device’s potential role in resource-limited settings. Participants are adults attending the glaucoma outpatient service who require visual field testing, and the study integrates into routine clinic activities with no additional follow-up beyond the trial visit. The trial seeks to understand practical use, feasibility, and performance in real-world conditions to inform future implementation in lower-income regions. Data will focus on how well WSFFM identifies significant field loss relative to HVF in this setting.

Why it matters

Potential benefit: If successful, WSFFM could offer a practical tool to help clinicians detect meaningful vision loss in glaucoma earlier, potentially guiding timely treatment or referrals.

How similar studies have gone: Previous work has explored field testing devices in glaucoma, but this pilot focuses on a novel device in a real-world, low-resource setting and is not designed to establish equivalence with HVF.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* \- Patients attending glaucoma outpatient clinic
* Patients requiring visual field testing, with plan for "SITA-STANDARD" HVF testing
* Patients 18 years or older and of any gender
* Patients capable of giving informed consent.

Exclusion Criteria:

* \- Patients not requiring visual field testing on that outpatient clinic attendance.
* Patients requiring visual field testing, with plan for "SITA-FAST" or "SITA-FASTER" HVF testing.
* Patients who do not attend their outpatient clinic appointment,
* Patients not able to perform visual field testing (for example due to their visual acuity, physical difficulty in positioning for test duration, or cognitive difficulties in understanding instructions).
* Patients under the age of 18 years old.

Where it's running

  • Buckinghamshire Healthcare NHS Trust
    Aylesbury, United Kingdom
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
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Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.