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Clinical Trials/KCT0003922
KCT0003922
Recruiting
未知

Prospective randomized clinical study on the effect of different number of intraocular lens haptics with or without a capsular tension ring on clinical outcomes after cataract surgery

Korea University Ansan Hospital0 sites40 target enrollmentTBD
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Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Korea University Ansan Hospital
Enrollment
40
Status
Recruiting
Last Updated
6 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional Study
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • •Subjects who voluntarily agreed to participate in the study after reading the clinical trial explanations and agreements, listening to the explanations for the study
  • •\-Subjects who visit Korea University Ansan Hospital by the IRB approval period and plan to undergo bilateral cataract surgery for cataract.
  • •\-Subjects who are 21 years of age or older
  • •\-Subjects who wish to undergo second cataract surgery between 1 and 4 weeks after the first cataract surgery
  • •\-Subjects who expected to have a best corrected visual acuity of 20/40 or better in the operated eye
  • •\-Subjects who have examinmation of biometry before cataract surgery using IOL Master®
  • •\-Subjects who have no opacity of the ocular medium except cataract.

Exclusion Criteria

  • •\- Subjects who have a disease that can affect vision
  • •\- Subjects who have amblyopia or strabismus
  • •\- Subjects who have an abnormality that can cause decentraion of the intraocular lens after cataract surgery
  • •\- Subjects who have corneal disease such as keratoconus and corneal dystrophy
  • •\- Subjects who have previous history of ocular trauma or refractive surgery
  • •\- Subjects who are using general medicine or eye drops that can affect vision.
  • •\- Subjects who are currently participating in other clinical studies or have participated in other clinical studies within 30 days of the strat day the study

Outcomes

Primary Outcomes

Not specified

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