Ireland
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Recruiting Observational

Evaluation of Cataract Surgery Outcome

NCT02182921 · tracked via the Priya Life Science China tracker
Phase
Observational
Started
2013-08
Last updated
2024-08-28

Condition(s) studied

CataractHigh Myopia

Study summary

The purpose of this study is to evaluate the visual outcome of the cataract surgery, including best uncorrected and corrected visual acuity, spherical equivalent, wavefront aberration and other measurements.

Eligibility

Sex
ALL
Min age
—
Max age
90 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)

  • Change from baseline in visual acuity at one month after cataract surgery — Follow-up until one month after surgery
  • Change from baseline in spherical equivalent at one month after cataract surgery — Follow-up until one month after surgery
  • Change from baseline in visual acuity at six months after cataract surgery — Follow-up until six months after surgery
  • Change from baseline in spherical equivalent at six months after cataract surgery — Follow-up until six months after cataract surgery

Trial sites (1)

FacilityCityRegionStatus
Eye and ENT Hospital of Fudan University Shanghai Shanghai Municipality Recruiting

More Evidence Based Cataract Study Group trials in China

Official registry record

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.

View NCT02182921 on ClinicalTrials.gov ↗ ← All trials in China