RecruitingACTRN12618001536257

Repeatability of central and peripheral eye length and choroidal thickness measurements in healthy subjects.


Sponsor

Brien Holden Vision Institute

Enrollment

40 participants

Start Date

Sep 8, 2017

Study Type

Observational

Conditions

Summary

This study aims to determine the repeatability of two investigational instruments ( the Lenstar LS 900 and the Triton Swept-source OCT). The instruments are used in optometric research to assess the length of the eye and the thickness of the vascular layer of the eye ( the choroid). To achieve this we wish to take measurements using the instruments over two separate days. The study sample will include a minimum of 15 participants to up to 40 participants with or without refractive errors, we wish to assess the repeatability of the instruments by taking two sets of measurements on two different days.


Eligibility

Sex: Both males and femalesMin Age: 18 Yearss

Plain Language Summary

Simplified for easier understanding

The length of the eye and the thickness of a layer inside the eye called the choroid can change over time and are important measurements in optometric research — particularly in understanding why some people become more short-sighted over their lives. Two instruments, the Lenstar LS 900 and the Triton Swept-source OCT, are used by eye researchers to take these measurements, but how consistent and repeatable their readings are has not been fully established. This study will simply take eye measurements using both instruments on two separate days (at least one day apart) and compare the results to determine how reliable the readings are. This is important so researchers know how much change in a measurement represents a true biological change versus just measurement variation. To be eligible you need to be 18 or older with normal eye health and either normal vision or a refractive error (short-sightedness, long-sightedness, or astigmatism). People with health conditions like diabetes, hypertension, or heart disease, or who have had eye surgery or used orthokeratology lenses, are not eligible. The study involves only non-invasive eye scans — no drops, medications, or procedures.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

This is a cross sectional and observational pilot study. The study sample will include participants with or without any refractive errors. The central and peripheral eye length and the thickness of th

This is a cross sectional and observational pilot study. The study sample will include participants with or without any refractive errors. The central and peripheral eye length and the thickness of the choroid will be analysed using the Lenstar LS 900 and the Triton Swept source OCT, respectively. The agreement between the readings obtained by both the instruments in two separate visits will be studied. The amount of time between visits will be between 1 to 40 days. The time between the visits will be determined based on the scheduling availability of the participant and the scheduling availability of equipment.


Locations(1)

NSW, Australia

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ACTRN12618001536257


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