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Study identifier: NCT05648474 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Intraoperative Monitoring for the Lateral Lumbar Interbody Fusion Procedure

Condition: Intervertebral Disc Degeneration · Stenosis, Spinal · Spondylolisthesis  ·  Sponsor: Alphatec Spine, Inc.

PhaseN/A
Planned participants400
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This study is designed to evaluate the clinical utility of a known intraoperative neuromonitoring modality (SSEP) using saphenous nerve as the site of stimulation to identify changes to the lumbar nerves which may be at risk during the lateral lumbar interbody fusion (LLIF) procedure.

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

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Contact details are listed per location below or on the registry record.

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Locations (1)

Alphatec Spine Inc.Carlsbad, California, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT05648474