Slidell, LANCT05504499Now EnrollingIRB Ready

Lumbar Spinal Stenosis Clinical Trial in Slidell, LA

Access cutting-edge lumbar spinal stenosis treatment through this clinical trial at a research site in Slidell. Study-provided care at no cost to qualified participants.

Sponsored by Pacific Research Institute

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Expert Care in Slidell

Access lumbar spinal stenosis specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related lumbar spinal stenosis treatment provided free

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Check if you qualify for this lumbar spinal stenosis clinical trial in Slidell, LA

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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 Slidell

    Convenient for LA 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 Slidell site if eligible
  4. 4Begin participation

About This Lumbar Spinal Stenosis Study in Slidell

The purpose of this study is to evaluate the effectiveness and safety of the use of Aurora Spine ZIP™ MIS Interspinous Fusion System and bone graft material in fusion in patients with chronic low back pain that present with degenerative disc disease with concurrent neurogenic claudication.

Sponsor: Pacific Research Institute

Who Can Participate

Inclusion Criteria

Subjects enrolled in this study must meet ALL of the following inclusion criteria:
Subject must provide written informed consent prior to any clinical study-related procedure.
Subject is at least 18 years or older at the time of enrollment, skeletal mature.
Subject has 1-2 symptomatic lumbar degenerative disease at adjacent level, T12-S1, with or without grade I spondylolisthesis (confirmed by history and radiographic studies).
MRI within 12 months prior to the procedure with at least mild to moderate spinal stenosis at the index treatment level
Subject has undergone at least 3 months of non-operative treatment.
Subject presents with ZCQ physical function ≥ 2.0 at baseline.
Subject reports relief from lumbar flexion and/or sitting.
Subject has baseline VAS of back and/or leg pain standing or walking ≥ 50mm.

Exclusion Criteria

Subjects enrolled in this study must NOT meet any of the following exclusion criteria:
Subject is unable to provide written informed consent.
Subject has had previous lumbar spine surgery at the intended treatment level (e.g., laminectomy or fusion).
Subject has a grade II or greater spondylolisthesis on flexion and extension radiographs with 3mm instability.
Subject has confirmed or suspected osteoporosis or osteopenia.
Subject is enrolled, or intends to participate, in a clinical drug and/or device study (investigational device, investigational drug, new indication for a device or drug, or additional testing beyond standard of care procedures) which could confound the results of this trial as determined by the investigator.
Presence of other anatomic or comorbid conditions, or other medical, social, or psychological conditions that, in the investigator's opinion, could limit the subject's ability to participate in the clinical investigation or to comply with follow-up requirements.
Subject is pregnant or nursing.

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 Slidell?

Yes, this clinical trial (NCT05504499) has an active research site in Slidell, LA 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.

Lumbar Spinal Stenosis Treatment Options in Slidell, LA

If you're searching for lumbar spinal stenosis treatment options in Slidell, LA, this clinical trial (NCT05504499) 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 Slidell research site is actively enrolling participants for this clinical trial. You'll receive care from experienced lumbar spinal stenosis 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 lumbar spinal stenosis clinical trials near you to find additional studies recruiting in your area.

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