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Massive french study reveals infection rates after common eye injections

NCT ID NCT03635268

Knowledge-focused Sponsor: Centre Hospitalier Universitaire Dijon 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at 360,000 French patients who received eye injections for conditions like age-related macular degeneration. The goal was to find out how often a serious eye infection called endophthalmitis happens within 28 days after the injection. Researchers analyzed data from 2007 to 2015 to understand the risks.

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

360,000 people

The number who actually took part.

Started

Jan 2016

Finished

Aug 2017

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

Patient who has had an intravitreal injection to deliver an anti-angiogenic agent or a corticosteroid

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: * adult patients within the French population who had an intravitreal injection, identified by CCAM coding BGLB001 * associated with the delivery of an anti-angiogenic agent or a corticosteroid, identified by the corresponding CIP code * between February 2007 and November 2015 Exclusion Criteria: * intraocular surgery less than 42 days before the first injection, identified by the CCAM procedure * risk factors for endogenous endophthalmitis identified in the 42 days preceding an IVI identified by the ICD10 code

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Conditions

The condition(s) this trial relates to.

age-related macular degeneration central retinal vein occlusion with macular edema diabetic macular edema

As listed by the trial registrant

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

Intravitreal injection

More trials for these conditions

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