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)
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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