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Randomized Trial Comparing Prediction Accuracy of Two Swept Source Optical Coherence Tomography Biometers

NCT05748275 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 80

Last updated 2024-09-19

Study results available
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Summary

To assess if the Alcon Argos Biometer utilizing the Barrett Universal II formula for IOL calculations can give a non-inferior outcome when compared to the Zeiss IOL master 700 utilizing the (PCA) with the Barrett Universal II (TK) formula, when comparing the (mean absolute prediction error of the predicted target spherical equivalencies).

Conditions

  • Cataract

Interventions

DIAGNOSTIC_TEST

Argos

Biometry measurements first with the Argos device, then the IOLMaster 700 device.

DIAGNOSTIC_TEST

IOLMaster 700

Biometry measurements first with the IOLMaster 700 device, then the Argos device.

Sponsors & Collaborators

  • Multack Eye Care

    lead OTHER

Principal Investigators

  • Sam Multack, D.O. · Multack Eye Care

Eligibility

Min Age
50 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-07-19
Primary Completion
2021-09-15
Completion
2021-09-15

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05748275 on ClinicalTrials.gov