NCT07298356

Brief Summary

Goldmann Applanation Tonometry (GAT) is considered the clinical gold standard for eye pressure measurements and yet it is known to be a subjective measurement with limited repeatability and limited portability. Another clinical standard for checking eye pressure is known as the pneumotonometer. This method is more objective but not portable. The purpose of this study is to develop new methods of measuring eye pressure that are more objective, reproducible and portable. In this study, the investigators will be comparing the eye pressure measurements using 2 investigational methods to GAT and pneuumotonometer.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
200

participants targeted

Target at P75+ for not_applicable

Timeline
8mo left

Started Mar 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress22%
Mar 2026Dec 2026

First Submitted

Initial submission to the registry

December 19, 2025

Completed
4 days until next milestone

First Posted

Study publicly available on registry

December 23, 2025

Completed
2 months until next milestone

Study Start

First participant enrolled

March 2, 2026

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 29, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 29, 2026

Last Updated

March 6, 2026

Status Verified

December 1, 2025

Enrollment Period

10 months

First QC Date

December 19, 2025

Last Update Submit

March 4, 2026

Conditions

Outcome Measures

Primary Outcomes (4)

  • Intraocular pressure (IOP) as measured by standard GAT

    this is the standard method for IOP measurement in clinical practice. The eye is given topical fluorescein/anesthetic, the GAT prism contacts the eye while the observer looks through the slit lamp machine ocular using blue light illumination to visual the applanation mires. The GAT dial is adjusted until mire alignment is achieved and the IOP measurement is read off the GAT dial.

    Baseline

  • Intraocular pressure (IOP) as measured by fixed force GAT

    From the patient perspective, this method will feel identical to the standard GAT. The eye is given topical fluorescein/anesthetic. The GAT dial is set at 1.8 or 2.0, a C-MOS camera is connected to one of the oculars of the slit lamp machine and under blue light illumination, the GAT prism contacts the eye while the CMOS camera makes a video of the mire appearance through the ocular.

    Baseline

  • Intraocular pressure as measured by upright applanating

    With this prototype, an applanating prism (custom manufactured with medical grade acrylic in an ISO-13485 certified facility) is attached to a fixed-force spring that creates a force equivalent to 1.8 or 2.0 on the GAT dial. Blue LED lights on the prototype are used to create the blue illumination similar to the blue light used in clinical practice on the slit lamp or Perkins tonometer. A C-MOS camera is aligned with the GAT prism to image the applanation mires. The eye is given topical fluorescein/anesthetic. Like fixed-force GAT, the GAT prism contacts the eye while the CMOS camera makes a video of the mire appearance. The diameters of the recorded mire images are measured and the IOP is calculated based on the mire diameter.

    Baseline

  • Intraocular pressure as measured by supine Pneumotonometer

    Baseline

Study Arms (4)

Standard GAT

ACTIVE COMPARATOR

This is the gold-standard method for IOP measurement in clinical practice

Device: Standard GAT

Fixed-force GAT

EXPERIMENTAL

From the patient perspective, this method will feel identical to the standard GAT. The eye is given topical fluorescein/anesthetic. The GAT dial is set at 1.8 or 2.0, a C-MOS camera is connected to one of the oculars of the slit lamp machine and under blue light illumination, the GAT prism contacts the eye while the CMOS camera makes a video of the mire appearance through the ocular. The diameters of the recorded mire images are measured and the IOP is calculated based on the mire diameter

Device: Fixed force GAT

Upright applanating prototype

EXPERIMENTAL

With this prototype, an applanating prism (custom manufactured with medical grade acrylic in an ISO-13485 certified facility) is attached to a fixed-force spring that creates a force equivalent to 1.8 or 2.0 on the GAT dial. Blue LED lights on the prototype are used to create the blue illumination similar to the blue light used in clinical practice on the slit lamp or Perkins tonometer. A C-MOS camera is aligned with the GAT prism to image the applanation mires. The eye is given topical fluorescein/anesthetic. Like fixed-force GAT, the GAT prism contacts the eye while the CMOS camera makes a video of the mire appearance. The diameters of the recorded mire images are measured and the IOP is calculated based on the mire diameter

Device: Upright applanating prototype

Pneumotonometer

ACTIVE COMPARATOR

This is another standard method for IOP measurement in clinical practice

Device: Pneumotonometer

Interventions

Standard Goldmann Applanation Tonometry (GAT): this is the standard method for IOP measurement in clinical practice

Standard GAT

An investigational device similar to standard GAT

Fixed-force GAT

An investigational device, prism used in standard and fixed-force GAT is attached to a portable device

Upright applanating prototype

This is a standard for checking eye pressure. A topical anesthetic (numbing agent). A probe will touch the front of the eye while the machine measures the eye pressure

Pneumotonometer

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Presenting for a routine eye exam
  • ≥ 18 years of age
  • Able and willing to give consent

You may not qualify if:

  • History of corneal scarring
  • Active infection of the eye
  • Ocular surface trauma or infection

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Duke Eye Center

Durham, North Carolina, 27710, United States

RECRUITING

MeSH Terms

Conditions

GlaucomaOcular Hypertension

Condition Hierarchy (Ancestors)

Eye Diseases

Study Officials

  • Joanne Wen, MD

    Duke Eye Center

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
DIAGNOSTIC
Intervention Model
PARALLEL
Model Details: In this 2 investigational methods (Fixed-force GAT and handheld tonometer) will be compared to the 2 standard methods (Standard GAT and pneumotonometer).
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

December 19, 2025

First Posted

December 23, 2025

Study Start

March 2, 2026

Primary Completion (Estimated)

December 29, 2026

Study Completion (Estimated)

December 29, 2026

Last Updated

March 6, 2026

Record last verified: 2025-12

Data Sharing

IPD Sharing
Will not share

No Currently, there is no plan to share data with other researchers.

Locations