Trials / Completed
CompletedNCT05290870
Registry Study on Intraocular Lenses Manufactured by Teleon Surgical B.V.
Registry Study on Hydrophilic (HydroSmart) and Hydrophobic (ACUNEX) Intraocular Lenses Manufactured by Teleon Surgical B.V.
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 2,183 (actual)
- Sponsor
- Teleon Surgical B.V. · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- —
Summary
This is a retrospective, observational (Registry) study aiming to collect safety and performance data on the use of intraocular lenses (IOLs) manufactured by Teleon Surgical B.V. according to routine practice.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Posterior-chamber intraocular lens | Implantation of a posterior-chamber intraocular lens to correct aphakia after removal of the crystalline lens |
Timeline
- Start date
- 2022-02-01
- Primary completion
- 2024-02-29
- Completion
- 2024-04-30
- First posted
- 2022-03-22
- Last updated
- 2024-07-03
Locations
1 site across 1 country: Netherlands
Source: ClinicalTrials.gov record NCT05290870. Inclusion in this directory is not an endorsement.