RecruitingNot ApplicableNCT05624398

Results of Patients With Glaucoma Undergoing Minimally Invasive Glaucoma Surgery in Conjunction With Cataract Surgery

Visual Outcomes and Patient Satisfaction in Subjects With Stable Open-angle Glaucoma Undergoing Concurrent Minimally Invasive Glaucoma Surgery and IOL Implantation With an Extended-depth-of-focus IOL


Sponsor

Vold Vision P.L.L.C

Enrollment

25 participants

Start Date

Dec 7, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

This study is designed to determine how well patients with glaucoma can see following cataract surgery with a special type of lens called an extended-depth-of-focus (EDOF) lens. This lens is intended to reduced the patients need for glasses following cataract surgery. Patients will also undergo a minimally invasive type of glaucoma surgery using a special type of stent to reduce eye pressure, with the goal of better glaucoma control and the reduction in the need for medications to control eye pressure.


Eligibility

Min Age: 45 Years

Plain Language Summary

Simplified for easier understanding

This study is tracking the outcomes of patients with mild glaucoma who have a small drainage device called a Hydrus Microstent implanted during routine cataract surgery. The goal is to see how well this minimally invasive procedure lowers eye pressure over time and reduces the need for glaucoma eye drops. **You may be eligible if...** - You are 45 or older with a visually significant cataract in both eyes - You have mild, stable open-angle glaucoma (a type affecting the drainage channels of the eye) - Your eye pressure is controlled on 1–3 glaucoma medications - Your glaucoma has been stable for at least 1 year - You are scheduled for cataract surgery **You may NOT be eligible if...** - You have had prior glaucoma surgery or laser treatment within 90 days - You have a more aggressive type of glaucoma (angle-closure, pseudoexfoliative, traumatic, neovascular) - You have moderate or severe glaucoma with significant vision field loss - You have other eye problems that could affect vision (like macular degeneration or significant corneal scarring) - You are pregnant or breastfeeding - You have had prior refractive surgery (LASIK, PRK, etc.) Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DEVICEVivity IOL

Cataract surgery with implantation of the Vivity IOL along with concurrent implantation of the Hydrus Microstent


Locations(1)

Vold Vision P.L.L.C.

Fayetteville, Arkansas, United States

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NCT05624398


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