Trials / Completed
CompletedNCT04907500
Prospective Evaluation of an Hydrophilic Acrylic Intraocular Lens
Prospective Evaluation of the Clinical Safety and Effectiveness of Hydrophilic Acrylic Intraocular Lens
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 387 (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 an hydrophilic acrylic intraocular lens
Detailed description
To show safety and the effectiveness in regard to the monocular corrected distance visual acuity (CDVA) and the distance-corrected near visual acuity (DCNVA) at 6 months postoperative.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Intraocular lens | Cataract surgery |
Timeline
- Start date
- 2021-06-22
- Primary completion
- 2022-08-06
- Completion
- 2022-12-16
- First posted
- 2021-05-28
- Last updated
- 2023-02-08
Locations
1 site across 1 country: Romania
Source: ClinicalTrials.gov record NCT04907500. Inclusion in this directory is not an endorsement.