Clinical Trials Logo

Aphakia clinical trials

View clinical trials related to Aphakia.

Filter by:

NCT ID: NCT01230060 Completed - Cataract Clinical Trials

One-Piece Hydrophobic Acrylic Intraocular Lens in Subjects Undergoing Cataract Extraction

Start date: October 2010
Phase: Phase 3
Study type: Interventional

The objective of this study is to evaluate the safety and effectiveness of the enVista® One-Piece Hydrophobic Acrylic intraocular lens (IOL), following primary implantation for the visual correction of aphakia in adults 18 years of age or older in whom the cataractous lens has been removed by an extracapsular cataract extraction method (eg, small incision phacoemulsification).

NCT ID: NCT01061281 Completed - Aphakia Clinical Trials

Evaluation of the Tecnis™ Multifocal and Crystalens™ Accommodating Intraocular Lenses

Start date: March 2010
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the visual outcomes with bilateral implantation of Tecnis MF and Crystalens™ AO Aberration-free Accommodating intraocular lens (IOLs) 6 months after post cataract surgery.

NCT ID: NCT00838045 Completed - Cataract Clinical Trials

Evaluation of the Safety & Effectiveness of the Bausch & Lomb AKREOS® TL Intraocular Lens

Start date: September 2006
Phase: Phase 4
Study type: Interventional

This study is to evaluate the safety and effectiveness of the Bausch & Lomb Akreos TL (thin lens) intraocular lens (IOL) following implantation in adults requiring cataract surgery.

NCT ID: NCT00773266 Completed - Aphakia Clinical Trials

Intraocular Position of Secondary Iris-Fixated IOLs in Aphakic Eyes

Start date: September 2006
Phase: N/A
Study type: Observational

The purpose of this study is to evaluate the intraocular stability and safety of secondary iris-fixated IOLs in aphakic patients.

NCT ID: NCT00625313 Completed - Aphakia Clinical Trials

Clinical Study of a UV-Absorbing Acrylic Posterior Chamber Intraocular Lens

HMY
Start date: March 2004
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the safety and efficacy of the HMY Model YA-60BB Intraocular Lens (IOL) when implanted in the posterior chamber of the human eye for the optical correction of aphakia following cataract extraction.

NCT ID: NCT00494390 Completed - Cataract Clinical Trials

Evaluation Study for a Non-Contact Biometer

Start date: July 2007
Phase: N/A
Study type: Observational

The purpose of this study is to determine whether a new non-contact biometer, is as accurate as the the available gold-standard.

NCT ID: NCT00212134 Completed - Congenital Cataract Clinical Trials

Infant Aphakia Treatment Study (IATS)

IATS
Start date: December 2004
Phase: N/A
Study type: Interventional

The primary purpose is to determine whether infants with a unilateral congenital cataract are more likely to develop better vision following cataract extraction surgery if they undergo primary implantation of an intraocular lens or if they are treated primarily with a contact lens. In addition, the study will compare the occurrence of postoperative complications and the degree of parental stress between the two treatments.