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Study reveals how eye damage tracks with vision decline in dry AMD

NCT ID NCT07424235

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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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study examined how vision loss progresses in people with geographic atrophy, an advanced form of dry age-related macular degeneration. Researchers analyzed past medical records and eye images from 60 patients to see which retinal changes are linked to faster vision decline. No treatments were tested—the goal was simply to better understand the disease's natural history.

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

60 people

The number who actually took part.

Started

Jan 2015

Finished

Dec 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

The study population consists of patients aged 50 years or older with geographic atrophy secondary to dry age-related macular degeneration, identified retrospectively from a single tertiary referral center. The analysis includes eyes meeting predefined anatomical and functional criteria similar to those used in recent clinical trials, based on clinical records and retinal imaging collected during routine care.

Ages

50 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: * Male or female patients aged 50 years or older at baseline. * Diagnosis of geographic atrophy secondary to dry age-related macular degeneration in the study eye. * Well-demarcated geographic atrophy lesions confirmed by fundus autofluorescence imaging, with a total lesion area between 2.5 mm² and 17.5 mm². * Presence of hyperautofluorescence in the junctional zone of the geographic atrophy lesion. * Best-corrected visual acuity between 45 and 83 ETDRS letters at baseline. * Availability of longitudinal clinical and imaging data with at least 6 months of follow-up. Exclusion Criteria: * Evidence or history of neovascular (wet) age-related macular degeneration in the study eye. * Prior intravitreal therapy or systemic treatments specifically targeting age-related macular degeneration. * Geographic atrophy lesions contiguous with peripapillary atrophy. * Coexisting ocular diseases that could independently affect visual acuity or retinal structure. * Incomplete or poor-quality clinical or imaging data precluding reliable assessment of study outcomes.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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