Comparison of the HSO iSert 251 Posterior Chamber Aspheric Aphakic Intraocular Lens to Historical and Literature Controls.



Status:Completed
Conditions:Ocular
Therapuetic Areas:Ophthalmology
Healthy:No
Age Range:50 - Any
Updated:5/27/2013
Start Date:February 2011
End Date:November 2012
Contact:James Wartman
Email:james.wartman@hoya.com
Phone:909-680-3900

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The purpose of this multi-center clinical trail is to determine the safety and efficacy of
the iSert 251 for the correction of aphakia.


Inclusion Criteria:

- Have been diagnosed with cataract for which phacoemulsification extraction and
posterior chamber IOL implantation is indicated

- Have clear intraocular media

- Have potential Best Corrected Visual Acuity of 20/40 or better

- Have preoperative Best Spectacle-Corrected visual acuity of 20/40 or worse

Exclusion Criteria:

- Have ocular pathology or abnormalities that do or are expected to reduce best
corrected visual acuity in the operative eye during the study period

- Are monocular

- Have current ocular infection

- Are taking systemic steroids or other anti-metabolites

- Have previous retinal detachment in the operative eye or expect to require retinal
laser treatment during the course of the study

Eligibility criteria not complete. Contact Hoya Surgical Optics, Inc. for more
information.
We found this trial at
5
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North Dartmouth, Massachusetts 02747
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Boynton Beach, Florida 33426
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Indianapolis, Indiana 46256
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Miami, Florida 33176
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8416 E. Shea Blvd., Ste C-101
Scottsdale, Arizona 85260
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Scottsdale, AZ
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