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

Part of paid clinical trials in Salt Lake City, Utah.

Sponsor
The Eye institute of Utah
Study ID
NCT06801678
Status
Recruiting
Apply to this trial

Conditions

  • Cataract

Eligibility Criteria

Sex
ALL
Age
21 Years - N/A
Healthy Volunteers
Not accepted

Study Details

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 Dates

Start date
Jan 9, 2025
Status verified
Jan 2025
Primary completion
Feb 7, 2025
Completion
Feb 22, 2025

Study Design

Enrollment
50 participants (estimated)

Arms

  • Arm: Observational
    No interventions will be administered.

Primary Outcome Measure

Differences in predicted refraction [ Time Frame: 1 month ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
The Eye Institute of UtahSalt Lake CityUtah84107
Lexi Guild
[email protected]
801-263-5705
Allison Hales
[email protected]
8012635735
Zachary J. Zavodni, MD (PRINCIPAL_INVESTIGATOR)

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