Trials / Recruiting
RecruitingNCT06428955
Evaluation of a Monofocal Intraocular Lens
Prospective Multicenter Evaluation of the Visual Performance of a Non-constant Aberration Correcting Aspheric Monofocal Intraocular Lens (Precise Study)
- Status
- Recruiting
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 44 (estimated)
- Sponsor
- Carl Zeiss Meditec AG · Industry
- Sex
- All
- Age
- 50 Years
- Healthy volunteers
- Accepted
Summary
The aim of this study is to investigate the 3-month visual performance of the CT LUCIA 621P IOL, a hydrophobic aspheric monofocal IOL with a non-constant aspheric optic profile in adult patients 50 years of age or older who are undergoing cataract surgery.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | CT LUCIA 621P | The device under investigation, CT LUCIA 621P IOL (Carl Zeiss Meditec, Jena, Germany) is a posterior chamber intraocular lens which is indicated for aphakia after surgical extraction of the cataractous natural lens. It is a monofocal aspheric IOL made of hydrophobic material and coated with heparin. The modified C-loop haptic is step-vaulted. |
Timeline
- Start date
- 2024-06-06
- Primary completion
- 2024-12-01
- Completion
- 2024-12-01
- First posted
- 2024-05-24
- Last updated
- 2024-06-24
Locations
4 sites across 2 countries: United States, Mexico
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT06428955. Inclusion in this directory is not an endorsement.