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ClinicalTrials.gov public records Last synced Nov 8, 2026, 8:08 PM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Showing 1–24 of 131 matching trials from the live ClinicalTrials.gov search.

Filters: Condition: Fusion of Spine Clear all

Conditions: Spinal Fusion, Spinal Stenosis, Scoliosis, Spondylolisthesis
Interventions: Optical 3D Scanner; Device
Lead sponsor: Advanced Scanners Inc.; Industry
Eligibility: Not listed
Enrollment: 2 participants
Healthy volunteers: Accepts healthy volunteers
Timeline: 2021
U.S. locations: 1
States / cities: Round Rock, Texas

Conditions: Lumbar Spinal Stenosis
Interventions: Stabilimax NZ® Dynamic Spine Stabilization System; Device
Lead sponsor: Applied Spine Technologies; Industry
Eligibility: 21 Years and older
Enrollment: 480 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2007 – 2010
U.S. locations: 19
States / cities: Phoenix, Arizona • Los Angeles, California • Oceanside, California + 16 more

Conditions: Pain, Postoperative
Interventions: Intravenous Acetaminophen, Placebo; Drug · Other
Lead sponsor: Children's Hospital of Philadelphia; Other
Eligibility: 10 Years to 18 Years
Enrollment: 67 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2011 – 2015
U.S. locations: 1
States / cities: Philadelphia, Pennsylvania

Conditions: Cervical Spine Fusion
Interventions: Anterior Cervical Discectomy & Fusion, Application of ADAM mechanoacoustic skin sensor; Procedure · Device
Lead sponsor: Northwestern University; Other
Eligibility: 18 Years to 88 Years
Enrollment: 11 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2021 – 2024
U.S. locations: 1
States / cities: Chicago, Illinois

Conditions: Spondylolisthesis
Interventions: Not listed
Lead sponsor: Zimmer Biomet; Industry
Eligibility: 20 Years to 80 Years
Enrollment: 38 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2006 – 2011
U.S. locations: 1
States / cities: Houston, Texas

Conditions: Degenerative Spondylolisthesis
Interventions: ART352-L; Biological
Lead sponsor: Ankasa Regenerative Therapeutics, Inc.; Industry
Eligibility: 50 Years and older
Enrollment: 12 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2020 – 2023
U.S. locations: 3
States / cities: Los Angeles, California • Rochester, Minnesota • Columbus, Ohio

Conditions: Spinal Fusion, Lumbar Discectomy
Interventions: Radiostereometric Analysis beads inserted during surgery; Procedure
Lead sponsor: State University of New York - Upstate Medical University; Other
Eligibility: 18 Years and older
Enrollment: 75 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: Started 2002
U.S. locations: 1
States / cities: Syracuse, New York

Conditions: Spinal Fusion
Interventions: NanoBone Bone Graft Substitute; Other
Lead sponsor: Artoss Inc.; Industry
Eligibility: 18 Years and older
Enrollment: 330 participants
Timeline: 2020 – 2025
U.S. locations: 6
States / cities: Chandler, Arizona • Tempe, Arizona • San Diego, California + 3 more

Conditions: Stenosis, Spondylosis, Degenerative Changes
Interventions: Accell Evo3 Prospective Use; Device
Lead sponsor: SeaSpine, Inc.; Industry
Eligibility: 18 Years and older
Enrollment: 30 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2012 – 2016
U.S. locations: 1
States / cities: Durango, Colorado

Conditions: Lumbar Degenerative Disc Disease, Spinal Stenosis, Spondylolisthesis, Spondylosis, Intervertebral Disk Displacement, Intervertebral Disk Degeneration, Spinal Diseases, Bone Diseases, Musculoskeletal Diseases, Spondylolysis
Interventions: NuCel, Demineralized Bone Matrix; Biological
Lead sponsor: OhioHealth; Other
Eligibility: 18 Years to 75 Years
Enrollment: 6 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2014 – 2017
U.S. locations: 2
States / cities: Columbus, Ohio

Conditions: Multimodal Analgesic Approach
Interventions: Ofirmev, Per Os Acetaminophen; Drug
Lead sponsor: Hospital for Special Surgery, New York; Other
Eligibility: 18 Years to 85 Years
Enrollment: 166 participants
Healthy volunteers: Accepts healthy volunteers
Timeline: 2017 – 2025
U.S. locations: 1
States / cities: New York, New York

Conditions: Spinal Fusion, Pain Management
Interventions: EXPAREL; Drug
Lead sponsor: Pacira Pharmaceuticals, Inc; Industry
Eligibility: 18 Years and older
Enrollment: 15 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2016 – 2017
U.S. locations: 3
States / cities: Miami, Florida • Columbus, Ohio • Philadelphia, Pennsylvania

Conditions: Spinal Fusion Acquired, Spinal Stenosis, Lesions of Lumbosacral Intervertebral Disc, Spinal Diseases
Interventions: Dexmedetomidine, 0.9% Saline; Drug
Lead sponsor: Vanderbilt University Medical Center; Other
Eligibility: 18 Years to 85 Years
Enrollment: 68 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2009 – 2012
U.S. locations: 1
States / cities: Nashville, Tennessee

Conditions: Intraoperative Hypotension
Interventions: E-Fusion Vasopressor Titration-Assist; Device
Lead sponsor: Autonomous Healthcare, Inc.; Industry
Eligibility: 22 Years and older
Enrollment: 10 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2027
U.S. locations: 1
States / cities: Winston-Salem, North Carolina

Conditions: Spine Surgery
Interventions: open label placebo; Other
Lead sponsor: Brigham and Women's Hospital; Other
Eligibility: 18 Years to 75 Years
Enrollment: 51 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2018 – 2020
U.S. locations: 1
States / cities: Boston, Massachusetts

Conditions: Cervical Spine Degeneration, ACDF Surgery
Interventions: Early PT, Delayed PT; Other
Lead sponsor: Vanderbilt University Medical Center; Other
Eligibility: 18 Years to 75 Years
Enrollment: 76 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2024 – 2027
U.S. locations: 4
States / cities: Honolulu, Hawaii • Nashville, Tennessee • Fort Sam Houston, Texas + 1 more

Conditions: Dysphagia After Anterior Cervical Decompression and Fusion of the Spine
Interventions: Dexamethasone, Saline; Drug · Other
Lead sponsor: NYU Langone Health; Other
Eligibility: 21 Years to 65 Years
Enrollment: 4 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2013 – 2015
U.S. locations: 3
States / cities: New York, New York • Westbury, New York

Conditions: Stenosis, Spondylosis, Degenerative Changes
Interventions: Demineralized Bone Matrix, rh-BMP2; Device
Lead sponsor: SeaSpine, Inc.; Industry
Eligibility: 18 Years and older
Enrollment: 43 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2011 – 2016
U.S. locations: 1
States / cities: Sacramento, California

Conditions: Degenerative Spine Disease
Interventions: FIBERGRAFT™ Aeridyan Matrix Bone Graft Substitute, Demineralized Bone Matrix; Device
Lead sponsor: DePuy Synthes Products, Inc.; Industry
Eligibility: 18 Years and older
Enrollment: 316 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2025 – 2029
U.S. locations: 5
States / cities: Sacramento, California • Chicago, Illinois • Lexington, Kentucky + 2 more

Conditions: Lumbar Spine Degeneration
Interventions: SpinalStim; Device
Lead sponsor: Orthofix Inc.; Industry
Eligibility: 18 Years and older
Enrollment: 206 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2017 – 2021
U.S. locations: 1
States / cities: Johnstown, Colorado

Conditions: Degenerative Disc Disease, Spine Fusion, Back Pain
Interventions: MagnetOs Easypack Putty, Demineralized Bone Matrix or Fibers mixed with local autograft bone; Device
Lead sponsor: Kuros Biosurgery AG; Industry
Eligibility: 18 Years and older
Enrollment: 60 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2024 – 2027
U.S. locations: 6
States / cities: Irvine, California • Grand Rapids, Michigan • St Louis, Missouri + 3 more

Conditions: Cervical Radiculopathy, Cervical Myelopathy
Interventions: Titan nanoLOCK interbody cage, ACDF interbody cage; Device
Lead sponsor: University of Texas Southwestern Medical Center; Other
Eligibility: 18 Years to 99 Years
Enrollment: 200 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2024 – 2026
U.S. locations: 1
States / cities: Dallas, Texas

Conditions: Degenerative Conditions of the Lumbar Spine, Lumbar Spinal Stenosis, Spondylolisthesis
Interventions: Minuteman G5 Device; Device
Lead sponsor: Spinal Simplicity LLC; Industry
Eligibility: 18 Years and older
Enrollment: 150 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2024 – 2030
U.S. locations: 7
States / cities: Newnan, Georgia • Indianapolis, Indiana • Kansas City, Kansas + 4 more

Conditions: Lumbar Radiculopathy
Interventions: Liposomal bupivacaine, Bupivacaine; Drug
Lead sponsor: Icahn School of Medicine at Mount Sinai; Other
Eligibility: 18 Years to 85 Years
Enrollment: 13 participants
Healthy volunteers: Healthy volunteers not accepted
Timeline: 2022 – 2024
U.S. locations: 1
States / cities: New York, New York

Search by objective public record fields.

Spine Registration Using 3D Scanning

Dynamic Stabilization for Lumbar Spinal Stenosis With Stabilimax NZ® Dynamic Spine Stabilization System

Analgesic Efficacy of Repeated Doses of Intravenous (IV) Acetaminophen in Post-operative Pediatric Spine Fusion Patients

Measuring Dysphagia After ACDF Surgery Through A Novel Wearable Sensor

Posterior Lateral Fusion (PLF) With Dynesys

Safety Evaluation of ART352-L in Subjects Undergoing Posterolateral Spinal Fusion

Use of Radiostereometric Analysis Beads (RSA) to Measure Motion in the Spine, Following Lumbar Spinal Surgery

Artoss Prospective Spine Registry Outcomes

Efficacy and Safety of Integra Accell Evo3 DBM in Instrumented Lumbar Spine Fusion

Human Amniotic Tissue-derived Allograft, NuCel, in Posteriolateral Lumbar Fusions for Degenerative Disc Disease

IV vs Oral Acetaminophen in Spine Fusion Perioperative Care

PK Study of EXPAREL in Subjects Undergoing Open Spinal Fusion or Reconstructive Surgery

Intraoperative Infusion of Precedex to Reduce Length of Stay After Lumbar Spine Fusion

Feasibility Study of E-Fusion Vasopressor Titration-Assist During Multi-Level Spine Surgery

Evaluation of Open-Label Conditioned Placebo Analgesia for Postoperative Opioid Reduction Following Spinal Fusion

Function After Anterior Cervical Discectomy and Fusion Surgery: Timing of Physical Therapy

Effect of Intravenous Corticosteroid Injections on Dysphagia After Cervical Spine Surgery

Efficacy and Safety of Accell Evo3 Demineralized Bone Matrix (DBM) in Instrumented Posterolateral Lumbar Spine Fusion

FIBERGRAFT Aeridyan Posterolateral Fusion Study

Study Using the SpinalStim Device Following Lumbar Fusion Surgery

Post Marketing Study of MagnetOs Easypack Putty Standalone Compared to Demineralized Bone Matrix or Fibers Mixed With Autograft in Patients Undergoing Posterolateral Lumbar Fusion

Prospective Comparative Analysis of ACDF vs Fusion Interbody Cages With nanoLOCK Osseointegrative Technology

Post-Market Clinical Study of Functional Motion Outcomes in Subjects Treated With the Minuteman Device

Erector Spinae Block for Spine Surgery