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New eye scanner put to the test in 55 people

NCT ID NCT04112472

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 tested a new device called EYESTAR 900 that uses light to measure the eye's shape and size. Researchers compared its accuracy to existing devices in 55 volunteers, including people with normal eyes and those needing cataract surgery. The goal was to see if the new device gives reliable measurements for planning eye surgeries.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
EYESTAR 900 optical biometry device
What this could lead to
If successful, this device could provide more accurate eye measurements for cataract surgery planning and other eye care.
What could go wrong
This is a small, early-stage device comparison study. It does not test a treatment or cure, and results may not lead to immediate clinical changes.

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.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

55 people

The number who actually took part.

Started

Jul 2019

Finished

Sep 2019

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

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

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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: At least one eye of each subject needs to fulfill one of the following inclusion criteria: * volunteers with normal phakic eye; * patients seeking cataract surgery; * patients with pseudophakic eye; * patients with oil-filled eye; * patients with aphakic eye. Exclusion Criteria: * Exclusion criteria per subject: * underage patients (younger than 18 years); * vulnerable patients; * inability to give informed consent; * Exclusion criteria per eye: * inability to maintain stable fixation; * corneal lesions or scarring; * previous corneal surgery (except: pseudophakic eyes, oil-filled eyes, aphakic eyes); * previous intraocular surgery (except: pseudophakic eyes, oil-filled eyes, aphakic eyes); * active inflammation of the eye; * active infection of the eye; * tear film break up time of less than 5 sec.

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As listed by the trial registrant

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

Contacts and locations

Locations

  • University Hopital Basel

    Basel, 4056, Switzerland

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