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Comparison of Methods for Assessing Intraocular Lens Position

NCT07218419 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 53

Last updated 2026-03-16

No results posted yet for this study

Summary

Prospective, multi-center, non-interventional, open label, clinical study.

Conditions

  • Tilt and Decentration

Interventions

DIAGNOSTIC_TEST

IOL Decentration Assessment

This study assesses two methods to measure IOL decentration. Each subject will be evaluated in only one eye with both methods for assessing IOL decentration: (i) retro-illuminated slit lamp image analysis (objective slit lamp method) and (ii) subjective slit lamp grading method. There is no treatment or intervention on this study.

Sponsors & Collaborators

  • Johnson & Johnson Surgical Vision, Inc.

    lead INDUSTRY

Principal Investigators

  • Surgical Vision Inc. Johnson and Johnson · Study Director

Eligibility

Min Age
22 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2025-11-03
Primary Completion
2026-01-16
Completion
2026-01-16
FDA Device
Yes

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 NCT07218419 on ClinicalTrials.gov