Actively Recruiting

Phase Not Applicable
Age: 40Years - 80Years
All Genders
NCT02678962

Comparison of Outcomes With Multifocal Intraocular Lenses

Led by Wenzhou Medical University · Updated on 2024-07-23

90

Participants Needed

1

Research Sites

539 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this study is to compare and evaluate the clinical outcomes of 6 kinds of Multifocal Intraocular Lenses: SN6AD1, SBL-3, LS-313 MF30, AT LISA tri 839 MP, ART, LS-313 MF30T.

CONDITIONS

Official Title

Comparison of Outcomes With Multifocal Intraocular Lenses

Who Can Participate

Age: 40Years - 80Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age from 40 to 80 years old, either gender
  • Patients with bilateral age related cataracts needing cataract surgery in both eyes
  • Willing to have second eye surgery within 7 days after first eye surgery
  • Expected postoperative visual acuity of 20/40 or better in both eyes
  • Corneal astigmatism measurements suitable for multifocal intraocular lens implantation
  • Ability to understand and willing to provide informed consent and attend study visits
Not Eligible

You will not qualify if you...

  • Existing eye diseases or conditions other than age related cataracts that prevent cataract surgery
  • Systemic diseases or conditions that could affect study results
  • History of eye surgery or eye trauma that could affect study results
  • Need for combined surgeries that could affect study results
  • Participation in another clinical trial within 30 days before this study
  • Use of systemic or eye medications that could affect study outcomes
  • Pregnant, breastfeeding, or planning to become pregnant during the study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

The Eye Hispital of Wenzhou Medical University

Wenzhou, Zhejiang, China, 325000

Actively Recruiting

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Research Team

A

AYong Yu, MD. PhD.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

6

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