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Trials / Completed

CompletedNCT07218419

Comparison of Methods for Assessing Intraocular Lens Position

Status
Completed
Phase
Study type
Observational
Enrollment
53 (actual)
Sponsor
Johnson & Johnson Surgical Vision, Inc. · Industry
Sex
All
Age
22 Years
Healthy volunteers
Accepted

Summary

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

Detailed description

The objective is to evaluate two methods for assessing IOL tilt and decentration in patients who have been unilaterally or bilaterally implanted with a refractive or diffractive nontoric TECNIS IOL before participating into this study. The agreement will be assessed between the decentration measurements derived from retro-illuminated slit lamp image analysis and those obtained from the subjective slit lamp grading method.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTIOL Decentration AssessmentThis 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.

Timeline

Start date
2025-11-03
Primary completion
2026-01-16
Completion
2026-01-16
First posted
2025-10-20
Last updated
2026-03-16

Locations

2 sites across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT07218419. Inclusion in this directory is not an endorsement.

Comparison of Methods for Assessing Intraocular Lens Position (NCT07218419) · Clinical Trials Directory