Trials / Completed
CompletedNCT04545671
Evaluation of a Trifocal Lens
Retro-prospective Evaluation of the Clinical Safety and Effectiveness of Hydrophilic Acrylic Intraocular Lens
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 389 (actual)
- Sponsor
- Carl Zeiss Meditec AG · Industry
- Sex
- All
- Age
- 45 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), the distance-corrected intermediate visual acuity (DCIVA) and the distance-corrected near visual acuity (DCNVA) at 12-24 month postoperative.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | trifocal lens | not applicable as patients are already implanted with the trifocal lens |
Timeline
- Start date
- 2020-11-01
- Primary completion
- 2022-03-16
- Completion
- 2022-03-16
- First posted
- 2020-09-11
- Last updated
- 2022-07-20
Locations
1 site across 1 country: Germany
Source: ClinicalTrials.gov record NCT04545671. Inclusion in this directory is not an endorsement.