Clinical Trials Directory

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

TypeNameDescription
DEVICEImplantation of an intraocular lensImplantation 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.