Trials / Unknown
UnknownNCT04226196
Rotational Stability of a Hydrophobic Acrylic Plate Haptic Intraocular Lens Using a Capsular Tension Ring - An Intraindividual Comparative Study
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 65 (estimated)
- Sponsor
- Medical University of Vienna · Academic / Other
- Sex
- All
- Age
- 45 Years – 95 Years
- Healthy volunteers
- Not accepted
Summary
The present study should investigate the influence of a capsular tension ring on postoperative rotational stability of a plate haptic hydrophilic acrylic intraocular lens. All patients will be operated on both eyes in one occasion. Both eyes receive a Zeiss 409MP plate haptic intraocular lens, while only on eye receives an additional capsular tension ring. Follow up visits take place 1 hour, 1 week, 1 month and 4 to 7 months after surgery. At the follow up visits, the actual IOL axis will be determined by retroillumination photography. IOL centration and tilt will be determined by anterior segment SS-OCT Casia II. IOLs will be implanted in 4 different axis 0 +/- 10 degrees, 45 +/- 10 degrees, 90 +/- 10 degrees, 135 +/- 10 degrees. IOL rotation, decentration and tilt then will be compared intraindividually.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Implantation of an intraocular lens | Implantation of an intraocular lens Zeiss 409 MP into the capsular bag using an injector, after removing of the human crystalline lens. |
Timeline
- Start date
- 2020-01-27
- Primary completion
- 2021-04-01
- Completion
- 2021-04-01
- First posted
- 2020-01-13
- Last updated
- 2020-04-15
Locations
1 site across 1 country: Austria
Source: ClinicalTrials.gov record NCT04226196. Inclusion in this directory is not an endorsement.