Analisa Arosemena, MD
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Analisa Arosemena, MD, outlines patient selection criteria for canaloplasty with the new iTrack Advance and discusses where she positions canaloplasty in her glaucoma treatment paradigm. She also highlights the unique advantages of the iTrack Advance, including its proprietary illuminated microcatheter tip.
Posted: 12/28/2023
Analisa Arosemena, MD
Analisa Arosemena, MD, outlines patient selection criteria for canaloplasty with the new iTrack Advance and discusses where she positions canaloplasty in her glaucoma treatment paradigm. She also highlights the unique advantages of the iTrack Advance, including its proprietary illuminated microcatheter tip.
Posted: 12/28/2023
Combined Canaloplasty and Cataract Surgery: Considerations for Implementation and Adoption
The Opportunity in Canaloplasty
Restoring the Anatomy with Canaloplasty
Understanding the Mechanisms Associated With Canaloplasty
Case Review: Canaloplasty in a Case of Steroid-Induced Uncontrolled Ocular Hypertension
The Versatility of Standalone Canaloplasty
Targeting and Treating All Glaucoma Anatomy with Canaloplasty
Pros Versus Cons of Preserving Trabecular Meshwork in the Treatment of Glaucoma: Part 2
Pros Versus Cons of Preserving Trabecular Meshwork in the Treatment of Glaucoma: Part 1
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With a legacy that spans more than 30 years in ophthalmology, Nova Eye Medical designs, develops, manufactures and markets a portfolio of proprietary glaucoma treatment technologies. Underpinning each of these technologies is our commitment to advance clinical outcomes and improve patient quality of life.
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The Nova Eye iTrack™ Advance is indicated for fluid infusion or aspiration during surgery.
The Nova Eye iTrack™ Advance is indicated for the cutting or disruption of the trabecular meshwork during goniotomy procedures.*
The Nova Eye iTrack™ Advance is indicated for catheterization and viscodilation of Schlemm’s canal to reduce intraocular pressure in adult patients with open-angle glaucoma.
* The iTrack™ Advance cutting function (goniotomy) is a Class 1 510(k) exempt device function that is not specifically indicated for the reduction of intraocular pressure (IOP) or the treatment of open-angle glaucoma.