Recruiting

Interspinous Fusion

Sponsor:

Pacific Research Institute

Code:

NCT05504499

Conditions

Lumbar Spinal Stenosis

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Accepted

Interventions

Interspinous Fusion

Study Details

Brief summary:

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.

Conditions

Lumbar Spinal Stenosis

Study ID

NCT05504499

Start date

Mar 19, 2021

Status verified date

Aug, 2022

Completion date

Jan 1, 2028

Anticipated

Primary completion date

Jan 1, 2028

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Accepted

Inclusion Criteria:

  • Subjects enrolled in this study must meet ALL of the following inclusion criteria:

1. Subject must provide written informed consent prior to any clinical study-related procedure.
2. Subject is at least 18 years or older at the time of enrollment, skeletal mature.
3. 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).
4. MRI within 12 months prior to the procedure with at least mild to moderate spinal stenosis at the index treatment level
5. Subject has undergone at least 3 months of non-operative treatment.
6. Subject presents with ZCQ physical function ≥ 2.0 at baseline.
7. Subject reports relief from lumbar flexion and/or sitting.
8. 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:

1. Subject is unable to provide written informed consent.
2. Subject has had previous lumbar spine surgery at the intended treatment level (e.g., laminectomy or fusion).
3. Subject has a grade II or greater spondylolisthesis on flexion and extension radiographs with 3mm instability.
4. Subject has confirmed or suspected osteoporosis or osteopenia.
5. 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.
6. 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.
7. Subject is pregnant or nursing.

Study Design

Enrollment

100 participants

Anticipated

Intervention Model

Single group

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Single Arm

A Prospective, Open-Label, Non-Randomized, Multi-Center Study Measuring Functional Outcomes In a Novel Interspinous Fusion Device In Subjects With Low Back Pain A Prospective, Observational, Open-Label, Non-Randomized, Multi-Center Study Measuring Functional Outcomes In a Novel Interspinous Fusion Device In Subjects With Low Back Pain

Interventions

Interspinous Fusion

The intended study population are adults 18 years or older with symptomatic lumbar degenerative disc disease resulting in back pain with lower extremity symptoms and neurogenic claudication that improves with spinal flexion who are candidates for use of the Zip™ MIS Interspinous Fusion device when undergoing spinal fixation procedures.

Primary outcome measure

  • To evaluate the efficacy and safety of the Aurora Spine ZIP™ MIS Interspinous Fusion System and bone graft material based on improvement in composite endpoints relative to baseline at 3 and 12 months 1. > 20mm pain reduction in VAS Back while standing [ Time Frame: 12 months ]

Central Contacts and Locations

Locations

The Raso Pain Center

Recruiting

Jupiter, Florida, United States, 33477

Contacts

Principal Investigator:

Louis Raso, MD

Koga Neurosurgery

Recruiting

Slidell, Louisiana, United States, 70458

Contacts

Principal Investigator:

Sebastian Koga, MD

National Spine and Pain Centers

Recruiting

Oxon Hill, Maryland, United States, 20745

Contacts

Principal Investigator:

Vipul Mangal, MD

Comprehensive & Interventional Pain Management

Recruiting

Henderson, Nevada, United States, 89509

Contacts

Principal Investigator:

Rainer Vogel, MD

Nevada Advanced Pain Specialists

Recruiting

Reno, Nevada, United States, 20745

Contacts

Principal Investigator:

Denis Patterson, DO

Reno Tahoe Pain Associates

Recruiting

Reno, Nevada, United States, 89509

Contacts

Principal Investigator:

Ali Nairizi, MD

The Pain Management Center

Recruiting

Voorhees, New Jersey, United States, 08043

Contacts

Principal Investigator:

Youseff Josephson, MD

Premier Pain Treatment Institute

Recruiting

Loveland, Ohio, United States, 45140

Contacts

Principal Investigator:

Michael Danko, MD

Center for Interventional Pain and Spine

Recruiting

Chadds Ford, Pennsylvania, United States, 17601

Contacts

Principal Investigator:

Steven Falowski, MD

More Information

Sponsor

Pacific Research Institute

Last update posted

Aug 18, 2022

Last verified

Aug, 2022

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Pacific Research Institute on 2022-08-18.