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Clinical Trials/NCT02183831
NCT02183831
Completed
Not Applicable

Comparison of Clinical Outcomes After Cataract Surgery With and Without Capsular Tension Ring

Yonsei University0 sites52 target enrollmentMay 2014
ConditionsCataract

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cataract
Sponsor
Yonsei University
Enrollment
52
Primary Endpoint
Best corrected visual acuity
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

This study was set up to identify clinical outcomes including a refractive shift or change in IOL calculation accuracy and optical quality after Ophtec® capsular tension ring in the eyes without zonular instability.

Registry
clinicaltrials.gov
Start Date
May 2014
End Date
June 2014
Last Updated
11 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • age between 40 and 79 years
  • no history of eye surgery or glaucoma
  • a transparent central cornea
  • pupil dilation at the preoperative examination of at least 6.0 mm
  • absence of biomicroscopic signs of pseudoexfoliation
  • normal fundus examination

Exclusion Criteria

  • presence of ocular disease that might affect the visual outcome (e.g., color vision disturbance, chronic uveitis)
  • presence of ocular disease that might affect contrast sensitivity function (e.g., glaucoma, maculopathy, high myopia)

Outcomes

Primary Outcomes

Best corrected visual acuity

Time Frame: 1 month after capsular tension ring and intraocular lens implantation (cataract surgery) using capsular tension ring

Visual acuity measurement using refractive error correction

refractive error

Time Frame: 1 month after capsular tension ring and intraocular lens implantation (cataract surgery) using capsular tension ring

Autokeratometry (KR-7100; Topcon, Tokyo, Japan) and manifested refraction were performed to examine refractive errors

Anterior chamber depth

Time Frame: 3 months after capsular tension ring and intraocular lens implantation (cataract surgery) using capsular tension ring

obtained with a Scheimpflug imaging system (Pentacam; OCULUS Optikgeräte GmbH, Wetzlar, Germany)

Ocular aberrations

Time Frame: 1month after capsular tension ring and intraocular lens implantation (cataract surgery) using capsular tension ring

measured using the ray-tracing aberrometer (iTrace, Tracey Technologies, Houston, TX, USA) at a pupil size of 5 mm in mesopic conditions, without pharmacologic dilatation

Secondary Outcomes

  • constrast sensitivity(3 months after capsular tension ring and intraocular lens implantation (cataract surgery) using capsular tension ring)
  • Best corrected visual acuity(3 months after capsular tension ring and intraocular lens implantation (cataract surgery) using capsular tension ring)
  • posterior capsular opacity grades(3 months after capsular tension ring and intraocular lens implantation (cataract surgery) using capsular tension ring)
  • refractive error(3 months after capsular tension ring and intraocular lens implantation (cataract surgery) using capsular tension ring)
  • Ocular aberrations(3 months after capsular tension ring and intraocular lens implantation (cataract surgery) using capsular tension ring)

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