Trials / Completed
CompletedNCT04998409
Evaluation of a Spherical Hydrophilic Acrylic Intraocular Lens
Retro-prospective Evaluation of the Clinical Safety and Effectiveness of Hydrophilic Acrylic Intraocular Lens
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 242 (actual)
- Sponsor
- Carl Zeiss Meditec AG · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Evaluation of the clinical safety and effectiveness of hydrophilic acrylic intraocular lens
Detailed description
To show safety and the effectiveness in regard to the monocular corrected distance visual acuity (CDVA) at 12-24 month postoperative.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Monofocal lens | not applicable as patients are already implanted with the monofocal lens |
Timeline
- Start date
- 2021-09-24
- Primary completion
- 2022-04-22
- Completion
- 2022-04-22
- First posted
- 2021-08-10
- Last updated
- 2022-05-05
Locations
1 site across 1 country: Germany
Source: ClinicalTrials.gov record NCT04998409. Inclusion in this directory is not an endorsement.