High MyopiaCataractVisual OutcomeGenetic Anticipation
Investigational drug(s) / intervention(s)
Cataract
Cataract: The genetic and environmental factors concerning to the pathogenesis of cataract in the three groups.
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 high myopic cataract and age-related cataract patients. The investigators will further investigate into the various genetic and environmental factors that may contribute to the pathogenesis of high myopic cataract.
Eligibility
Sex
ALL
Min age
20 Years
Max age
100 Years
Healthy volunteers
No
Inclusion Criteria:
* Clinical diagnosis of 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 clinical phenotypes and visual outcomes of high myopic cataract patients — Follow-up until five years after surgery Cataract type and severity of high myopic cataract patients are evaluated using LOCSIII grading system. Visual outcomes are also evaluated including visual acuity with or without correction, intraocular pressure, fundus function, contrast sensitivity and other visual outcome measurements.
Differences in the clinical phenotypes and visual outcomes of age-related cataract patients — Follow-up until five years after surgery Cataract type and severity of age-related cataract patients are evaluated using LOCSIII grading system. Visual outcomes are also evaluated including visual acuity with or without correction, intraocular pressure, fundus function, contrast sensitivity and other visual outcome measurements.
Differences in the clinical phenotypes and visual outcomes of ametropic cataract patients — Follow-up until five years after surgery Cataract type and severity of ametropic cataract patients are evaluated using LOCSIII grading system. Visual outcomes are also evaluated including visual acuity with or without correction, intraocular pressure, fundus function, contrast sensitivity and other visual outcome measurements.
Trial sites (1)
Facility
City
Region
Status
Eye and ENT Hospital of Fudan University
Shanghai
Shanghai Municipality
Recruiting
More Shanghai High Myopia 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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