intraocular lens implantation: 1)Pediatric cataract patients with intraocular lens implantation and those without intraocular lens implantation;2)Traumatic cataract patients with intraocular lens implantation and those without intraocular lens implantation
Study summary
The purpose of this study is to evaluate the long-term visual outcome of the cataract surgery using a large-scale and comprehensive database of pediatric cataract participants, including congenital and traumatic cataract. The investigators will further investigate into the various genetic and environmental factors that may contribute to the pathogenesis of pediatric cataract.
Eligibility
Sex
ALL
Min age
2 Months
Max age
20 Years
Healthy volunteers
No
Inclusion Criteria:
* Clinical diagnosis of pediatric cataract
* Must be able to cooperate with the ophthalmic examination
Exclusion Criteria:
* Clinical diagnosis of mental illness
* Mentally disabled
Primary outcome measure(s)
Differences in the visual outcomes of pediatric cataract patients. — Follow-up until ten years after surgery. Visual outcomes are evaluated including visual acuity with or without correction, refractive changes, intraocular pressure, fundus function, fixation type, vision development, growth of axial length, contrast sensitivity and other visual outcome measurements.
Genetic diversity based on biospecimen samples of pediatric cataract patients. — Analyzed within six months after surgery. Sequencing of genes (including exons, promoters, 5' UTR and 3' UTR sequences) on a large scale to intensively investigate into the sites and functions of single nucleotide polymorphism (SNP) correlated with clinical features of congenital cataract patients, compared to traumatic cataract patients.Samples of blood, aqueous humor, anterior capsular membranes and lens tissues were applied for the genetic analysis.
Trial sites (1)
Facility
City
Region
Status
Eye and ENT Hospital of Fudan University
Shanghai
Shanghai Municipality
Recruiting
More Evidence Based Cataract Study Group trials in China
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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