Beaumont, TXNCT07465913Now EnrollingIRB Ready

Glaucoma Clinical Trial in Beaumont, TX

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

Sponsored by Eye Centers of Southeast Texas

Quick Self-Assessment

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Expert Care in Beaumont

Access glaucoma specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related glaucoma treatment provided free

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Check if you qualify for this glaucoma clinical trial in Beaumont, TX

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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 Beaumont

    Convenient for TX 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 Beaumont site if eligible
  4. 4Begin participation

About This Glaucoma Study in Beaumont

This is a randomized, double-masked, single-site, prospective, contralateral eye study designed to evaluate the outcomes of Direct Selective Laser Trabeculoplasty (DSLT) followed by the addition of combination netarsudil and latanoprost (Rocklatan) versus latanoprost monotherapy. The study will be conducted at one investigational site. The primary endpoint is the change in mean diurnal intraocular pressure (IOP) from baseline (post DSLT and post washout) at visit 3 between the two groups. Secondary endpoints include the change in mean IOP from baseline at each timepoint (8am, 12pm, 4pm) at visit 3 between groups, and the mean percentage decrease in IOP from baseline for each group. Assessments will be conducted at three key visits: Visit 1 (Screening Phase and DSLT Procedure on Day 0), Visit 2 (Baseline Visit post washout at Week 8), and Visit 3 (Follow-Up Visit 1 at Week 12). Each visit will include specific examinations and measurements such as visual field and OCT imaging, diurnal IOP measurements, and documentation of adverse events.

Sponsor: Eye Centers of Southeast Texas

Who Can Participate

Inclusion Criteria

Adults (≥18 years) with a diagnosis of mild to moderate bilateral primary open-angle glaucoma (POAG) or open-angle glaucoma (OAG).
On 3 topical glaucoma medications at screening, one of which must be a prostaglandin analog.
Post-DSLT and post-washout, baseline intraocular pressure (IOP) 16-36 mmHg in both eyes.
Best-corrected visual acuity (BCVA) ≥20/60 in both eyes.
Ability and willingness to provide informed consent.

Exclusion Criteria

Ocular hypertension only (no glaucomatous damage).
Inability or medical ineligibility for washout of ocular hypotensive medications.
Prior selective laser trabeculoplasty (SLT) within 12 months of screening.
History of glaucoma surgery (trabeculectomy, tube shunt, minimally invasive glaucoma surgery \[MIGS\] affecting outflow).
Narrow or closed angles with gonioscopy (Shaffer grading ≤2).
Active ocular infection, uveitis, or severe dry eye.
Corneal pathology interfering with IOP measurement.
Advanced glaucoma (threat to fixation).
Known hypersensitivity to Rocklatan, latanoprost, or study medication components.
Pregnancy or lactation.

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 Beaumont?

Yes, this clinical trial (NCT07465913) has an active research site in Beaumont, TX 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 Treatment Options in Beaumont, TX

If you're searching for glaucoma treatment options in Beaumont, TX, this clinical trial (NCT07465913) 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 Beaumont research site is actively enrolling participants for this clinical trial. You'll receive care from experienced glaucoma 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 clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Beaumont, TX