Development of an IT Tool Able to Identify Ocular Conditions

Aston University

Status

Withdrawn

Conditions

Eye Diseases

Treatments

Diagnostic Test: Measurement of corneal biomechanical properties

Study type

Observational

Funder types

Other

Identifiers

NCT05973617

005-2021-SN

Details and patient eligibility

About

The aim of the study is to use machine learning to develop an IT tool able to differentiate between eye conditions analysing corneal biomechanical data.

Full description

Data will be collected using two different commercially available devices that are able to measure corneal biomechanics. Corneal biomechanics will be measured in participants with different conditions: glaucoma, ocular hypertension, corneal conditions, and healthy controls as it is well established that the above-mentioned conditions cause changes in corneal biomechanical properties.

Corneal biomechanics are the mechanical properties of the cornea, as rigidity, elasticity and it is possible to measure them using two devices: Ocular Response Analyzer (ORA) or Corneal Visualization Scheimpflug Technology (Corvis ST). Both devices use a puff of air to temporally flatten the cornea and derive the properties of the tissue.

Participants with ocular conditions will be recruited at Birmingham and Midlands Eye Centre (BMEC) at the Glaucoma and Anterior Eye clinics among patients attending for their routine clinical appointment. Healthy controls will be recruited at Aston University. This study requires only one visit and there is no need of follow up.

A portion of the data collected will be used to train machine learning algorithms to differentiate between conditions, the remaining data will be used to test the accuracy of newly created algorithms. The algorithm will be developed using Orange Data Mining.

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Age above 18 years old.
Participants who are able to give informed consent.
Study groups: Patients with diagnosis of glaucoma or corneal disease or ocular hypertension. Patients that are having a treatment (medications or surgery) for glaucoma or ocular hypertension or corneal conditions.
Control group: people with no diagnosis or treatment of previous pathologies.

Exclusion criteria

Age below 18.
Participants who are not able to give informed consent.
Patients with eye conditions not within the inclusion criteria.
Patients with respiratory distress or significant head tremor.
Patients who are in pain or unable to remain seated for duration of measurements.
Participants that during the visit are wearing contact lenses. The wear of contact lenses can alter the measure of corneal biomechanics.