AccuraSee™ IOPCL for Improved Near Vision After Cataract Surgery

This study is testing a device called the AccuraSee™ intraocular pseudophakic capsular lens (IOPCL) to see if it can safely and effectively improve your near and/or intermediate vision after you've already had cataract surgery. You might be able to join if you are 22 years or older and have previously had cataract surgery with specific types of Alcon or Johnson and Johnson monofocal lenses. The researchers will know if the device is successful by measuring improvements in your uncorrected near vision (how well you see up close without glasses) at 12 months. The current status of this study is unclear, and it plans to enroll 10 participants.

Study design
This is an interventional study, meaning participants will receive a specific treatment. It plans to enroll 10 participants.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Participants will be followed for at least 12 months to measure improvements in their near vision.

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NCT06625749

Evaluate the Safety and Effectiveness of the AccuraSee™ IOPCL for Secondary Implantation in the Capsular Bag to Improve Near and/or Intermediate Vision Following Previous Cataract Surgery

Recruiting
NAAges 22+InterventionalTreatment
OnPoint Vision Inc
~10 participants
Updated 2024-10-03 on ClinicalTrials.gov
What's tested:Accurasee™ IOPCL

At a glance

Recruiting sites
1 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Improvement in uncorrected near visual acuity (UCNVA) at 40 cm/16 inches
Measured over 12 months
Refractive Surgery
Refractive Error - Myopia
1 sites across 1 states
Ohio1

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  • Improvement in uncorrected near visual acuity (UCNVA) at 40 cm/16 inches12 months

    Improvement in uncorrected near visual acuity (UCNVA) (at 40 cm/16 inches) at 12 months postoperatively. At least 75% of treated eyes should achieve an uncorrected near visual acuity (UCNVA) of 20/32 or better.