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Eye-Opening study: do two Pre-Cataract scanners agree?

NCT ID NCT07500272

Knowledge-focused Sponsor: Burapha University Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study checked how well two different devices (OA-2000 and Pentacam AXL) agree when measuring the eye before cataract surgery. 94 cataract patients had their eyes measured once with each device. The goal was to see if the devices give the same numbers for lens power and eye shape, which helps surgeons pick the right implant.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

94 people

The number who actually took part.

Started

Sep 2024

Finished

Nov 2024

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Participants diagnosed with cataracts and scheduled for cataract surgery at the Ophthalmology Outpatient Department, Burapha University Hospital, Chonburi, Thailand

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Participants aged 18 years or older, diagnosed with cataracts and scheduled for cataract surgery Exclusion Criteria: * History of corneal trauma * Prior ocular surgery * The use of contact lenses within two weeks of measurement * The presence of other concurrent ocular pathologies

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Conditions

The condition(s) this trial relates to.

cataract lens disorder

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Cataract Intraocular lens

Contacts and locations

Locations

  • Burapha University

    Chon Buri, 20131, Thailand

More trials for these conditions

Other studies related to the condition(s) this trial covers.