Trials / Unknown
UnknownNCT05596682
Prospective Multicenter Clinical Study on the Visual and Refractive Outcomes and Safety Outcomes Following Implantation of an AddOn Intraocular Lens in Previously Pseudophakic Eyes
- Status
- Unknown
- Phase
- —
- Study type
- Observational
- Enrollment
- 75 (estimated)
- Sponsor
- Medicontur Medical Engineering Ltd · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this prospective multicenter clinical study is to evaluate the visual and refractive outcomes and safety outcomes following bilateral implantation of trifocal and/or trifocal toric 1stQ AddOn (Medicontur) intraocular lenses (IOLs) to correct residual refractive errors, astigmatism, and presbyopia in previously pseudophakic eyes.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | supplementary intraocular lenses | Implantation of supplementary intraocular lenses into the ciliary sulcus in previously pseudophakic eyes. |
Timeline
- Start date
- 2022-10-17
- Primary completion
- 2024-05-31
- Completion
- 2024-08-31
- First posted
- 2022-10-27
- Last updated
- 2023-06-02
Locations
4 sites across 4 countries: Belgium, France, Spain, United Kingdom
Source: ClinicalTrials.gov record NCT05596682. Inclusion in this directory is not an endorsement.