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Objective Assessment of Intraocular Lens Tilt and Decentration

NCT07324200 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 80

Last updated 2026-05-08

No results posted yet for this study

Summary

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

Conditions

  • Tilt and Decentration

Interventions

DIAGNOSTIC_TEST

OCT Imaging Test

The primary objective of this study is to evaluate the repeatability and reproducibility (R\&R) of a method based on Optical Coherence Tomography (OCT) image analysis for assessing IOL tilt and decentration in patients unilaterally or bilaterally implanted with TECNIS refractive or diffractive non-toric IOL models.

Sponsors & Collaborators

  • Johnson & Johnson Surgical Vision, Inc.

    lead INDUSTRY

Principal Investigators

  • Surgical Vision Inc. Johnson and Johnson · Sponsor GmbH

Eligibility

Min Age
22 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-03-03
Primary Completion
2026-06-26
Completion
2026-06-26
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 NCT07324200 on ClinicalTrials.gov