Actively Recruiting

Age: 21Years +
All Genders
NCT06801678

Refractive Outcomes Utilizing Two SS-OCT Biometers for IOL Power Calculations

Led by The Eye institute of Utah · Updated on 2025-01-30

50

Participants Needed

1

Research Sites

6 weeks

Total Duration

On this page

Sponsors

T

The Eye institute of Utah

Lead Sponsor

A

Alcon Research

Collaborating Sponsor

AI-Summary

What this Trial Is About

The purpose of this study is to evaluate and compare the potential refractive outcomes using the Argos 1.5 biometer in the surgical planning for cataract extraction to that obtained from IOLMaster 700. Both devices are used as standard of care in surgical planning optimization for patients undergoing cataract surgery.

CONDITIONS

Official Title

Refractive Outcomes Utilizing Two SS-OCT Biometers for IOL Power Calculations

Who Can Participate

Age: 21Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 21 years or older
  • Diagnosed with Cataract Grade 1 or higher in at least one eye according to LOCS III or Wisconsin Grading scale
  • Able to understand and sign the informed consent form
  • Expected postoperative best corrected distance visual acuity of 0.3 logMAR or better with targeted emmetropia based on investigator's medical opinion
Not Eligible

You will not qualify if you...

  • No active ocular infection or inflammation
  • Unable to fixate due to nystagmus or other significant eye movement abnormalities
  • Contraindicated for pupil dilation due to conditions like narrow angles or allergies as judged by the investigator
  • Presence of any ocular disease or condition that may pose significant risk, affect study results, or interfere with participation according to the investigator's clinical judgment

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 Institute of Utah

Salt Lake City, Utah, United States, 84107

Actively Recruiting

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Research Team

L

Lexi L Guild

CONTACT

A

Allison Hales

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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