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Intraocular Lens Rotation clinical trials

View clinical trials related to Intraocular Lens Rotation.

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NCT ID: NCT06294405 Recruiting - Lens Opacities Clinical Trials

Intraocular Lens Implant Registry Study

Start date: February 21, 2024
Phase:
Study type: Observational [Patient Registry]

The goal of this registry study is to optimize the results with intraocular lens implants used in cataract surgery.

NCT ID: NCT05530473 Completed - Clinical trials for Intraocular Lens Rotation

Combined Capsular Tension Ring and IOL Implantation for Management of Cataracts

Start date: January 1, 2020
Phase: N/A
Study type: Interventional

This study included cataract patients who underwent intraocular lens (IOL) implantation with or without capsular tension ring (CTR), which aimed to evaluate the contribution of the use of CTR in clinical visual outcomes and rotational stability of IOL after cataract surgery.

NCT ID: NCT04226196 Recruiting - Clinical trials for Intraocular Lens Rotation

Rotational Stability of a Hydrophobic Acrylic Plate Haptic Intraocular Lens Using a Capsular Tension Ring - An Intraindividual Comparative Study

ConTRol
Start date: January 27, 2020
Phase: N/A
Study type: Interventional

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.