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A Post-market Clinical Study to Collect Safety and Performance Data on Johnson & Johnson Surgical Vision Products

NCT05394324 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1674

Last updated 2025-07-20

No results posted yet for this study

Summary

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

Conditions

  • Refractive Error
  • Glaucoma
  • Cataracts
  • Clear Lens Exchange

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 subject devices 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
2022-06-21
Primary Completion
2025-05-31
Completion
2025-05-31
FDA Device
Yes

Countries

  • United States
  • Germany
  • Spain

Study Locations

More Related Trials

Entities

Diseases

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 NCT05394324 on ClinicalTrials.gov