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Evaluation of Real-World Data on the Performance of the TECNIS Odyssey™ IOL

NCT05991960 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 96

Last updated 2024-02-02

No results posted yet for this study

Summary

Retrospective collection of data from medical records, multicenter, post-market clinical follow-up study.

Conditions

  • Cataracts

Interventions

DEVICE

Intervention

No study treatments will be administered during this retrospective study. However, data will be collected from medical records of patients who have been treated with the subject device of this study.

Sponsors & Collaborators

  • Johnson & Johnson Surgical Vision, Inc.

    lead INDUSTRY

Principal Investigators

  • Johnson & Johnson Surgical Vision, Inc. Clinical Trial · Johnson & Johnson Surgical Vision, Inc.

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-09-11
Primary Completion
2023-12-04
Completion
2023-12-04
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 NCT05991960 on ClinicalTrials.gov