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600 Kids' eye surgeries tracked for a decade: what happens next?

NCT ID NCT07087275

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 This study
Running, but no longer taking on new participants.
Completed
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 follows 600 children aged 0-16 who had cataract surgery after an eye injury. Researchers will check vision, eye growth, and complications over 5-10 years to understand long-term healing and guide better care. No new treatment is tested—just careful observation of past surgeries.

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

About 600 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jun 2010

Expected to finish

Jun 2030

An estimate. End dates often move.

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

This study will enroll pediatric patients aged 0 to 16 years who were diagnosed with traumatic cataract and underwent cataract surgery at the Eye, Ear, Nose, and Throat Hospital of Fudan University, or the Eye Hospital of Wenzhou Medical University, or the First Affiliated Hospital of Nanjing Medical University. Eligible patients may have experienced either blunt or penetrating ocular trauma. Both unilateral and bilateral cases are included. All participants must be able to complete regular follow-up evaluations for at least 5 years after surgery. The study population reflects a broad spectrum of post-traumatic cataract severity and treatment modalities, representing real-world clinical settings.

Ages

Up to 16 years

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 1. Aged 0 to 16 years at the time of trauma-related cataract diagnosis 2. Diagnosed with traumatic cataract (due to blunt or penetrating ocular trauma) 3. Underwent cataract extraction surgery with or without intraocular lens (IOL) implantation 4. Able to attend regular follow-up assessments for at least 5 years postoperatively 5. Written informed consent obtained from a parent or legal guardian Exclusion Criteria 1. Congenital or developmental cataract 2. Pre-existing ocular diseases unrelated to trauma (e.g., congenital glaucoma, retinal dystrophies) 3. Severe posterior segment damage precluding reliable visual outcome evaluation (e.g., endophthalmitis, choroidal rupture involving the macula) 4. Systemic or neurological disorders that affect vision or compliance with follow-up (e.g., cerebral palsy, intellectual disability) 5. Previous intraocular surgery in the affected eye unrelated to the trauma

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

Contacts and locations

Locations

  • Eye and ENT hospital of Fudan University

    Shanghai, Shanghai Municipality, 200000, China