Fayetteville, ARNCT05624398Now EnrollingIRB Ready

Glaucoma, Open-Angle Clinical Trial in Fayetteville, AR

Access cutting-edge glaucoma, open-angle treatment through this clinical trial at a research site in Fayetteville. Study-provided care at no cost to qualified participants.

Sponsored by Vold Vision P.L.L.C

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Expert Care in Fayetteville

Access glaucoma, open-angle specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related glaucoma, open-angle treatment provided free

Apply for This Fayetteville Location

Check if you qualify for this glaucoma, open-angle clinical trial in Fayetteville, AR

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Fayetteville

    Convenient for AR residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Fayetteville site if eligible
  4. 4Begin participation

About This Glaucoma, Open-Angle Study in Fayetteville

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.

Sponsor: Vold Vision P.L.L.C

Who Can Participate

Inclusion Criteria

Male or female subjects 45 years of age or older
A visually significant age-related cataract in both eyes
Diagnosis of mild OAG
VF characteristics consistent with glaucoma with mean deviation not worse than -6.00 dB and without fixation threatening scotoma AND/OR with nerve abnormalities consistent with glaucoma (rim notching, rim thinning, disc hemorrhage, nerve fiber layer loss)
Medicated IOP ≤25 mmHg on 1-3 hypotensive medications
Glaucoma must be judged as stable by investigator based on review of subject medical records
Stable VF at least 1 year prior to surgery
Stable nerve fiber layer at least 1 year prior to surgery
IOP stable on current medication regimen at least 3 months prior to surgery
Shaffer grade of ≥ III in all angle quadrants
Potential of best corrected visual acuity at distance in the investigator's judgement of at least 0.1 logMAR (20/25) postoperatively
Able and willing to comply with follow up visits
Understands and signs the informed consent
Both eyes of the subject should undergo surgery within 21 days of each other to ensure adequate timing for final visit window of 90 days ± 21 days post operatively

Exclusion Criteria

Previous incisional glaucoma surgery or cilio-ablative surgery
Prior laser trabeculoplasty within 90 days of surgery
Pseudoexfoliative, angle closure, uveitic, congenital, traumatic, angle recession, or neovascular glaucoma.
Moderate glaucoma with VF mean deviation between -6.00 dB and -12.00 dB
Severe and/or progressive glaucoma defined as
VF mean deviation worse than -12.00 dB
Consistent worsening of visual field on review of subject medical records
Consistent and progressive thinning of nerve fiber layer on review of subject medical records
Uncontrolled IOP on maximum glaucoma medications
Historically poor IOP control with medical therapy
Severe focal notching of the optic nerve rim
Expectation for future need of incisional glaucoma surgery
Ocular pathology or other medical condition which, in the investigator's judgment places the subject at increased risk of complications or significant vision loss during study period
Ocular pathology that in the investigator's judgment may impact visual acuity postoperatively, i.e., significant ocular surface disease, corneal scarring, blepharitis, epiretinal membrane, macular degeneration, history of significant ocular trauma with sequela, etc.
Pregnant or breastfeeding women
Prior refractive surgery e.g., LASIK, RK, PRK, etc.
Subjects with significant complications during surgical procedure e.g., broken capsule, Hydrus Microstent complication, will be exited from the trial
Subjects who experience visually significant complications related to the Hydrus Microstent during the study period will be exited from the trial

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Fayetteville?

Yes, this clinical trial (NCT05624398) has an active research site in Fayetteville, AR that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Glaucoma, Open-Angle Treatment Options in Fayetteville, AR

If you're searching for glaucoma, open-angle treatment options in Fayetteville, AR, this clinical trial (NCT05624398) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Fayetteville research site is actively enrolling participants for this clinical trial. You'll receive care from experienced glaucoma, open-angle specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all glaucoma, open-angle clinical trials near you to find additional studies recruiting in your area.

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