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A Multicenter, Observational, Single Arm Study of the TECNIS Presbyopia-correcting Intraocular Lens

NCT06250322 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 307

Last updated 2026-04-13

No results posted yet for this study

Summary

Ambispective post-market data collection on visual symptoms, patient satisfaction and surgeon experience with the TECNIS PC IOL.

Conditions

  • Cataracts

Interventions

DEVICE

Intervention

No study treatments will be administered during this 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
2024-04-10
Primary Completion
2025-06-30
Completion
2025-06-30
FDA Device
Yes

Countries

  • Australia
  • Austria
  • France
  • Germany
  • India
  • Netherlands
  • South Korea
  • Spain

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 NCT06250322 on ClinicalTrials.gov