No phaseCompletedAge-related condition
Clinical Study of a UV-Absorbing Acrylic Posterior Chamber Intraocular Lens (HMY)
A Prospective, Multi-center, Single-phase, Non-randomized, Open-label Study to Assess the Safety and Efficacy of the HMY Model YA-60BB Intraocular Lens (IOL) for the Correction of Aphakia Following Phacoemulsification Cataract Extraction
- Sponsor
- Hoya Surgical Optics, Inc. (Industry)
- Enrolment
- 617 enrolled
- Conditions
- Aphakia
- Interventions
- HMY Model YA-60BB IOL
- Ages
- adults, older adults
- Registry
- NCT00625313
Full record on ClinicalTrials.gov
From the registry
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.
Primary outcomes
- Best Corrected Visual Acuity
History
Last registry update
Primary completion
Registered
Started