Trials / Completed
CompletedNCT06250322
A Multicenter, Observational, Single Arm Study of the TECNIS Presbyopia-correcting Intraocular Lens
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 307 (actual)
- Sponsor
- Johnson & Johnson Surgical Vision, Inc. · Industry
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
Ambispective post-market data collection on visual symptoms, patient satisfaction and surgeon experience with the TECNIS PC IOL.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| 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. |
Timeline
- Start date
- 2024-04-10
- Primary completion
- 2025-06-30
- Completion
- 2025-06-30
- First posted
- 2024-02-09
- Last updated
- 2026-04-13
Locations
20 sites across 8 countries: Australia, Austria, France, Germany, India, Netherlands, South Korea, Spain
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT06250322. Inclusion in this directory is not an endorsement.