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Study identifier: NCT02272140 Synced from ClinicalTrials.gov · August 08, 2026
● Study status: Completed

Advanced XLIF Monitoring Multicenter Study

Condition: Degenerative Lumbar Disc Disease  ·  Sponsor: NuVasive

PhaseN/A
Planned participants324
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNoCheck eligibility criteria ↓
Where12 locations

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

The objective of this study is to evaluate the utility of localized stimulation of the lumbosacral nerve roots during XLIF through correlation of observed changes in the response latency, amplitude, waveform morphology, and/or response threshold with surgical events. Additionally, correlation between neuromonitoring findings and postoperative neural status will be evaluated.

This description comes directly from the study's public registry record.

Talk to the study team

No contact information is available for this study as per the public registry record.

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Full eligibility criteria (exactly as the study team wrote them)

Inclusion Criteria: 1. Male and female spine surgery patients who are at least 18 years of age; 2. Persistent back and/or leg pain unresponsive to conservative treatment for at least six (6) months, unless surgical treatment is clinically indicated earlier; 3. Surgical candidates for extreme lateral approach lumbar spine surgery at spinal levels L2 to L5, inclusive of L4-5; 4. Able to undergo surgery based on physical exam, medical history and surgeon judgment; 5. Patients who understand the conditions of enrollment and are willing to sign an informed consent to participate in the evaluation. Exclusion Criteria: 1. Patient has a mental or physical condition that would limit the ability to comply with study requirements; 2. Currently undergoing any surgical treatment at any spinal level other than L2 to L5; 3. Currently undergoing surgical treatment for significant deformity correction (e.g., osteotomy, anterior longitudinal ligament release, or other significant manipulation of the spinal column); 4. Underlying neurological disease or neurological deficit that is not associated with the condition for which he/she is seeking surgical intervention (e.g., diabetic peripheral neuropathy); 5. Implanted pacemaker, defibrillator, or other electronic devices; 6. Involved in active litigation relating to the spine (worker's compensation claim is allowed if it is not contested); 7. Pregnant women; 8. Patient is a prisoner; 9. Patient is participating in another clinical study that would confound study data.

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (12)

Scripps Clinical Research ServicesLa Jolla, California, United States
USF Neurology and NeurosurgeryTampa, Florida, United States
Foundation for Orthopaedic Research and Education (FORE)Tampa, Florida, United States
Piedmont HealthcareAtlanta, Georgia, United States
West Augusta Spine Specialists, LLCAugusta, Georgia, United States
Massachusetts General HospitalBoston, Massachusetts, United States
Columbia Orthopedic Group ResearchColumbia, Missouri, United States
Western Regional Center for Brain & Spine SurgeryLas Vegas, Nevada, United States
Duke University Medical CenterDurham, North Carolina, United States
University of Pittsburgh Medical CenterPittsburgh, Pennsylvania, United States
Seton Brain and Spine InstituteAustin, Texas, United States
Northwest Orthopaedic Specialists, P.S.Spokane, Washington, United States

More studies in these areas

This study lists sites in the areas below. Each link shows other recruiting studies near that city, from the public registry record.

La JollaTampaAtlantaAugusta

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