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

Study Status: Completed
Recruit Status: Completed
Study Type: Interventional

Official Title: A Prospective, Multi-Center Clinical Investigation to Evaluate the Safety & Effectiveness of the Bausch & Lomb AKREOS® TL (Model MI60) Intraocular Lens

Brief Summary: 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.

Detailed Summary:
Sponsor: Bausch & Lomb Incorporated

Current Primary Outcome: Bast Corrected Visual Acuity [ Time Frame: 24 months ]

best-corrected visual acuity (BCVA)


Original Primary Outcome: Safety and effectiveness of the Bausch & Lomb Akreos TL intraocular lens. [ Time Frame: 24 months ]

Current Secondary Outcome:

  • Uncorrected Visual Acuity [ Time Frame: 24 months ]
  • Manifest Refraction [ Time Frame: 24 Months ]
    mean manifest refraction


Original Secondary Outcome:

Information By: Bausch & Lomb Incorporated

Dates:
Date Received: February 5, 2009
Date Started: September 2006
Date Completion:
Last Updated: December 7, 2011
Last Verified: December 2011