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Epidemiology and Outcome of Pediatric Traumatic Cataract

A

Assiut University

Status

Completed

Conditions

Traumatic Cataract

Treatments

Procedure: traumatic cataract extraction

Study type

Observational

Funder types

Other

Identifiers

NCT04630509
Pediatric traumatic cataract

Details and patient eligibility

About

this study aims to explore the demography of pediatric traumatic cataract in upper Egypt, and report outcomes and complications of traumatic cataract surgery in these children.

Full description

Ocular trauma is one of the leading causes of acquired unilateral blindness in childhood.1,2 Apart from the permanent disability, ocular trauma has a profound impact on both patients and society at different levels, including, but not limited to, psychological trauma, cosmetic disfigurement, socioeconomic costs, and the need for specialized medical care and vocational rehabilitation.

Traumatic cataract is a common complication of pediatric eye injury. In developing countries, ocular trauma was responsible for up to 45% of childhood cataract. Vision loss induced by traumatic cataract is surgically manageable. However, the high risk of postoperative inflammation, posterior capsular opacification (PCO), amblyopia, and the associated ocular tissue damage may negatively impact visual outcome.

Several studies reported visual outcome of pediatric traumatic cataract in different populations. With the sacristy of studies on traumatic cataract in Egyptian children, we conducted this retrospective study to report the demographic features, visual outcome, and complications of pediatric traumatic cataract at Assiut University Hospital, the biggest tertiary referral center in Upper Egypt.

Enrollment

34 patients

Sex

All

Ages

Under 17 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All children who have undergone traumatic cataract surgery at Assiut university over 1 year period.

Exclusion criteria

  • children with posterior segment injury.
  • children who did not complete at least 6 months of postoperative follow-up.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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