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User Acceptability Evaluation of Pseudophakic Patients Previously Implanted With the TECNIS Odyssey IOL

NCT06005675 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 44

Last updated 2025-04-25

No results posted yet for this study

Summary

Prospective 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 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
2023-09-06
Primary Completion
2024-05-01
Completion
2024-05-01
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 NCT06005675 on ClinicalTrials.gov