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Intraocular Lens

Minimally Invasive Glaucoma Surgery + Cataract Surgery for Glaucoma

N/A
Recruiting
Research Sponsored by Vold Vision P.L.L.C
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 3 months
Awards & highlights
No Placebo-Only Group

Summary

This trial tests a lens to reduce need for glasses and a stent to reduce glaucoma meds after cataract surgery.

Who is the study for?
This trial is for adults over 45 with mild open-angle glaucoma and age-related cataracts, without severe vision loss or eye surgery history. Participants should have stable glaucoma and be on up to three pressure-lowering meds. They must be able to see well after surgery and follow the study schedule.
What is being tested?
The study tests how a special lens implant (Vivity IOL) during cataract surgery affects vision in glaucoma patients. It also examines the effects of a minimally invasive stent procedure aimed at reducing eye pressure and medication needs post-surgery.
What are the potential side effects?
Potential side effects may include discomfort, redness, or inflammation in the eye; temporary blurred vision; increased eye pressure requiring additional treatment; or rare complications from the stent placement.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 3 months for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Mean Photopic Monocular Best Corrected Distance Visual Acuity (DCVA) (4 meters) logMAR
Secondary study objectives
Mean Absolute Prediction Error
Mean Photopic Binocular Best Corrected Distance Visual Acuity (DCVA) (4 meters) logMAR
Mean Photopic Binocular Best Distance Corrected Intermediate Visual Acuity (DCIVA) (66 cm) logMAR
+7 more
Other study objectives
IOL patient satisfaction (IOLSAT) questionnaire
Mean Mesopic Binocular Best Corrected Distance Low Contrast Visual Acuity (25%) (4 meters) logMAR
Mean Photopic Binocular Best Corrected Distance Low Contrast Visual Acuity (25%) (4 meters) logMAR
+6 more

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups
Experimental Treatment
Group I: Treatment GroupExperimental Treatment1 Intervention
Subjects implanted with the Vivity IOL undergoing concurrent implantation of the Hydrus Microstent
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Vivity IOL
2020
N/A
~90

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Open-Angle Glaucoma treatments primarily aim to reduce intraocular pressure (IOP) to prevent optic nerve damage. Medications like prostaglandin analogs and beta-blockers either increase aqueous humor outflow or decrease its production. Laser therapies, such as Selective Laser Trabeculoplasty (SLT), enhance the drainage of aqueous humor through the trabecular meshwork. Minimally invasive glaucoma surgeries (MIGS), including the use of glaucoma stents, improve aqueous humor outflow by creating new drainage pathways. Extended-Depth-of-Focus (EDOF) lenses, while primarily used to improve vision post-cataract surgery, can be combined with MIGS to provide comprehensive care by addressing both vision correction and IOP management. These treatments are vital for glaucoma patients as they help maintain vision and prevent disease progression.
Effect of topical prostaglandin D2 on the aqueous humor dynamics in rabbits.

Find a Location

Who is running the clinical trial?

Vold Vision P.L.L.CLead Sponsor
1 Previous Clinical Trials
25 Total Patients Enrolled
Alcon ResearchIndustry Sponsor
731 Previous Clinical Trials
128,884 Total Patients Enrolled

Media Library

Vivity IOL (Intraocular Lens) Clinical Trial Eligibility Overview. Trial Name: NCT05624398 — N/A
Primary Open Angle Glaucoma Research Study Groups: Treatment Group
Primary Open Angle Glaucoma Clinical Trial 2023: Vivity IOL Highlights & Side Effects. Trial Name: NCT05624398 — N/A
Vivity IOL (Intraocular Lens) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05624398 — N/A
~2 spots leftby Feb 2025