MedPath

Evaluation of Cataract Surgery Outcome

Recruiting
Conditions
High Myopia
Cataract
Registration Number
NCT02182921
Lead Sponsor
Evidence Based Cataract Study Group
Brief 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.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
20000
Inclusion Criteria
  • Clinical diagnosis of cataract
  • Must be able to cooperate with the ophthalmic examination
Exclusion Criteria
  • Clinical diagnosis of mental illness
  • Mentally disabled

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Change from baseline in spherical equivalent at six months after cataract surgeryFollow-up until six months after cataract surgery
Change from baseline in visual acuity at one month after cataract surgeryFollow-up until one month after surgery
Change from baseline in spherical equivalent at one month after cataract surgeryFollow-up until one month after surgery
Change from baseline in visual acuity at six months after cataract surgeryFollow-up until six months after surgery
Secondary Outcome Measures
NameTimeMethod
Change from baseline in intraocular light scattering at one month after cataract surgeryFollow-up until one month after surgery
Change from baseline in intraocular light scattering at six months after cataract surgeryFollow-up until six months after surgery
Change from baseline in wavefront aberration at one month after cataract surgeryFollow-up until one month after surgery
Change from baseline in contrast sensitivity at one month after cataract surgeryFollow-up until one month after surgery
Change from baseline in contrast sensitivity at six months after cataract surgeryFollow-up until six months after surgery
Change from baseline in wavefront aberration at six months after cataract surgeryFollow-up until six months after surgery

Trial Locations

Locations (1)

Eye and ENT Hospital of Fudan University

🇨🇳

Shanghai, Shanghai, China

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