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

Recruiting now

Conditions studied: Cataract

In brief

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.

Key facts

Study ID

NCT06801678

Run by

The Eye institute of Utah

People needed

50

Starts

2025-01-09

Expected to finish

2025-02-22

Last updated by the study team

2025-01-30

Who can join

Age: 21 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 21 years or older (Adult age)
• Assessed to have Cataract Grade 1 and above per LOCS III or Wisconsin Grading scale in at least one eye.
• Able to comprehend and sign the informed consent form.
• Potential postoperative best corrected distance visual acuity (BCDVA) of 0.3 logMAR or better and targeted post-op refraction to be emmetropia, based on the investigator expert medical opinion.

You may not qualify if…

• No active ocular infection or inflammation
• Unable to fixate due to nystagmus or other eye movement abnormality (e.g., significant strabismus)
• Contraindicated for pupil dilation (e.g., narrow angles, allergies) per medical judgement of the investigator.
• Any ocular disease and/or condition that, in the investigator's clinical judgment, may put the subject at significant risk, may compromise study result or may interfere significantly with the subject's participation in the study.

Where it is running

• The Eye Institute of Utah — Salt Lake City, Utah, United States (enrolling)

Full record on ClinicalTrials.gov

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