About this trial
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 criteria
This trial does not accept healthy volunteersQualifiers
Clinical diagnosis of cataract
Must be able to cooperate with the ophthalmic examination
Disqualifiers
Clinical diagnosis of mental illness
Mentally disabled
Trial population
Medical centre: Eye and ENT Hospital of Fudan University
Trial design
Case-control
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Change from baseline in visual acuity at one month after cataract surgery
Change from baseline in spherical equivalent at one month after cataract surgery
Change from baseline in visual acuity at six months after cataract surgery
Change from baseline in spherical equivalent at six months after cataract surgery
Secondary outcomes
Change from baseline in wavefront aberration at one month after cataract surgery
Change from baseline in contrast sensitivity at one month after cataract surgery
Change from baseline in intraocular light scattering at one month after cataract surgery
Change from baseline in wavefront aberration at six months after cataract surgery
Other outcomes
The difference between attempted and achieved refractive correction at one month after cataract surgery
The difference between attempted and achieved refractive correction at six months after cataract surgery
Sponsors and contacts
Click on the lead sponsor to view all of their trials.