Clinical trial Recruiting at 1 site Observational Ages 21 and up

Comparing two devices for measuring eye parameters in cataract surgery

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

Run by The Eye institute of Utah · NCT06801678 · Data updated 2026-11-12

This study is testing which of two devices is better at measuring eye parameters to help adults with cataracts get the best vision after surgery.

Quick facts

Study typeObservational
Ages21 Years and up
SexAll
Enrollment50 (estimated)
SponsorThe Eye institute of Utah
Academic / other
Locations1 site (Salt Lake City, Utah)
StatusRecruiting
StartedJanuary 9, 2025
Main results expectedFebruary 7, 2025
Study endsFebruary 22, 2025
Registry record updatedJanuary 30, 2025
Trial IDNCT06801678 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults aged 21 and older with cataract grade 1 or higher in at least one eye.

Probably not a fit

Patients with active ocular infections, significant eye movement abnormalities, or contraindications for pupil dilation may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study evaluates and compares the refractive outcomes of cataract surgery using two different optical biometers: the Argos 1.5 and the IOLMaster 700. Both devices are standard in surgical planning for cataract extraction, and the study aims to determine which device provides more accurate intraocular lens (IOL) power calculations. Accurate measurement of ocular parameters is crucial for achieving optimal postoperative visual outcomes. The study will include adults with cataracts and assess their potential for achieving emmetropic vision post-surgery.

Why it matters

Potential benefit: If successful, this study could enhance the accuracy of IOL power calculations, leading to improved visual outcomes for cataract surgery patients.

How similar studies have gone: Previous studies have shown success with similar biometry approaches, indicating potential for meaningful advancements in cataract surgery outcomes.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* 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.

Exclusion Criteria:

* 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's running

  • The Eye Institute of Utah
    Salt Lake City, Utah, United States
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
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Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.