Actively Recruiting

Age: 20Years - 100Years
All Genders
ID03062085

Visual Outcome Evaluation and Genetic Analysis: Shanghai High Myopia Study

Led by Shanghai High Myopia Study Group · Updated on 2026-05-11

60000

Participants Needed

1

Research Sites

521 weeks

Total Duration

On this page

Sponsors

S

Shanghai High Myopia Study Group

Lead Sponsor

E

Eye & ENT Hospital of Fudan University

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research aims to evaluate the long-term visual outcomes after cataract surgery in patients with high myopia compared to those with age-related cataract and ametropic cataract. It focuses on understanding the differences in clinical features and prognosis among these groups. Additionally, the study investigates genetic and environmental factors that may contribute to the development and progression of high myopic cataract using a large-scale clinical database. Participants are grouped into three categories: high myopic cataract, age-related cataract, and ametropic cataract patients. Researchers will analyze genetic variations by sequencing selected genes related to cataract pathogenesis, vitreoretinopathy, and postoperative complications. The study uses comprehensive clinical data and biological samples to explore single nucleotide polymorphisms and their correlation with clinical characteristics. During the study, participants will undergo ophthalmic examinations and follow-up evaluations for up to five years after surgery to assess visual outcomes. Genetic diversity will be analyzed within six months post-surgery. The study monitors clinical phenotypes, visual results, and genetic markers to better understand the disease and improve prevention and prognosis. Participant involvement includes clinical assessments and sample collection, and the study duration spans from surgery through long-term follow-up.

CONDITIONS

Brief Title

Shanghai High Myopia Study

Who Can Participate

Age: 20Years - 100Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Clinical diagnosis of cataract
  • Ability to cooperate with ophthalmic examinations
  • Age between 20 and 100 years
Not Eligible

You will not qualify if you...

  • Clinical diagnosis of mental illness
  • Mental disability

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Diagnostic Evaluation

Duration - Up to surgery date

Participants undergo ophthalmic examinations and genetic analysis related to cataract and myopia.

1 visit (in-person)

Long-term Monitoring

Duration - Up to 5 years after surgery

Participants are followed for up to five years after cataract surgery to evaluate visual outcomes and clinical phenotypes.

Regular follow-up visits over 5 years

Trial Site Locations

Total: 1 location

1

Eye and ENT Hospital of Fudan University

Shanghai, Shanghai Municipality, China, 200031

Actively Recruiting

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Research Team

Y

Yi Lu, M.D.

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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Published Research Related To This Trial

Role of Optic Nerve Head Characteristics in Predicting Intraocular Pressure Spikes after Cataract Surgery in Highly Myopic Eyes.

Wenwen He, Ling Wei, Shuyu Liu...

https://pubmed.ncbi.nlm.nih.gov/37178442

Measurement of crystalline lens tilt in high myopic eyes before cataract surgery using swept-source optical coherence tomography.

Qiang Lu, Wenwen He, Dongjin Qian...

https://pubmed.ncbi.nlm.nih.gov/32161773