| OLIF25™ /OLIF51™ Study (NCT02657421) | Medtronic Spinal and Biologics | 2015-11-01 |
| New Robotic Assistance System for Spinal Fusion Surgery (NCT02558621) | KB Medical SA | 2015-09-01 |
| Placebo-controlled Study to Evaluate Rexlemestrocel-L Alone or Combined With Hyaluronic Acid in Participants With Chronic Low Back Pain (NCT02412735) | Mesoblast, Ltd. | 2015-03-06 |
| Evaluation of the Effectiveness of Spa Treatment in Swieradow Zdroj With Special Regard to the Action of Radon Waters (NCT03274128) | Wroclaw Medical University | 2015-03-01 |
| Clinical Evaluation of GENEX® DS in Instrumented Posterolateral Fusion (NCT02317185) | Spine Wave | 2014-12-01 |
| Efficacy of Intradiscal Injection of Viable Placental Tissue Extract in Subjects With One or Two Level, Symptomatic Lumbar Intervertebral Disc Degeneration (NCT02379689) | Semmes-Murphey Foundation | 2014-12-01 |
| Phase 2a Study on Allogeneic Osteoblastic Cells Implantation in Lumbar Spinal Fusion (NCT02205138) | Bone Therapeutics S.A | 2014-10-01 |
| Comparison of Complication Rates Between Lateral Approaches to the Lumbar Spine (NCT02068729) | K2M, Inc. | 2014-06-01 |
| Facet Wedge Post Market Study (NCT02203448) | Synthes GmbH | 2014-05-01 |
| Restore CLINICAL TRIAL (NCT01609374) | Spinal Kinetics | 2014-05-01 |
| Annex™ Adjacent Level System for Treatment of Adjacent Level Disease (NCT02108249) | Spine Wave | 2014-04-01 |
| Adipose Cells for Degenerative Disc Disease (NCT02097862) | Bioheart, Inc. | 2014-03-01 |
| Post-Market Surveillance Study of the TM Ardis Interbody Fusion System (NCT02429908) | Zimmer Biomet | 2014-03-01 |
| Safety and Efficacy of the CarboFix Pedicle Screw System (NCT02039232) | CarboFix Orthopedics Ltd. | 2014-01-01 |
| Personalized Spine Study Group Registry (NCT03843476) | Medicrea, USA Corp. | 2014-01-01 |
| A Retrospective Study Using CALIBER® TLIF Expandable Spacer in the Treatment of DDD: 2 Year Follow-up. (NCT02388022) | Globus Medical Inc | 2014-01-01 |
| Retrospective/Prospective Data Collection on the LDR ROIA Interbody Fusion Device With VerteBRIDGE Plating (NCT02104141) | LDR Spine USA | 2013-11-01 |
| The Prevalence of Bone Degenerative Diseases in Beijing - a Cross-sectional Study (NCT03086109) | Beijing Jishuitan Hospital | 2013-10-01 |
| Retrospective/Prospective Data Collection on the LDR ROIC Interbody Fusion Device With VerteBRIDGE Plating (NCT02104167) | LDR Spine USA | 2013-09-01 |
| Utilization of Autologous Mesenchymal Cells in Posterolateral Spinal Fusion in Degenerative Spine Disease (NCT03827096) | Bioinova, s.r.o. | 2013-08-27 |
| Multicenter Study of the Avenue L Interbody Spinal Fusion System Using VerteBRIDGE Plating and Posterior Fixation (NCT02068768) | LDR Spine USA | 2013-07-15 |
| Treatment of Degenerative Disc Disease With Allogenic Mesenchymal Stem Cells (MSV) (NCT01860417) | Red de Terapia Celular | 2013-06-21 |
| Prospective Study To Assess The Safety and Efficacy of the PROW LIF Procedure (NCT01850537) | NLT Spine | 2013-05-01 |
| Assessment of nanOss Bioactive 3D in the Posterolateral Spine (NCT01829997) | Pioneer Surgical Technology, Inc. | 2013-04-01 |
| Clinical and Radiological Outcomes of Oblique Lateral Lumbar Interbody Fusion (NCT03726190) | Tristate Brain and Spine Institute | 2013-01-01 |
| Outcomes of Degenerative Disc Disease Patients Treated With an Anterior-Only Fusion Using InQu Bone Graft (NCT01746212) | Kansas Joint and Spine Institute | 2012-12-01 |
| A Study Comparing the Safety and Effectiveness of Cartilage Cell Injected Into the Lumbar Disc as Compared to a Placebo (NCT01771471) | ISTO Technologies, Inc. | 2012-11-01 |
| Study of an Expandable Interbody Device for the Lumbar Spine (NCT02075554) | Globus Medical Inc | 2012-07-01 |
| Minuteman Spinal Fusion Implant Versus Surgical Decompression for Lumbar Spinal Stenosis (NCT01455805) | Spinal Simplicity LLC | 2012-06-01 |
| RAMP Study: A Study Comparing Two Lumbar Fusion Procedures (NCT01716182) | Baxano Surgical, Inc. | 2012-06-01 |
| Safety, Tolerability and Efficacy of YH14618 in Patients With Degenerative Disc Disease (NCT01526330) | Yuhan Corporation | 2012-05-01 |
| Outcome Analysis for Minimally Invasive Spine Surgery and Navigation (NCT01751841) | Weill Medical College of Cornell University | 2012-05-01 |
| INDEPENDENCE Spacer for Lumbar Fusion (NCT02299323) | Globus Medical Inc | 2012-01-01 |
| Safety and Preliminary Efficacy Study of Mesenchymal Precursor Cells (MPCs) in Subjects With Lumbar Back Pain (NCT01290367) | Mesoblast, Ltd. | 2011-08-01 |
| PEEK and Allograft Spacers Evaluation in Spinal Fusion Surgeries (NCT01406405) | Justin Parker Neurological Institute | 2011-07-01 |
| Intervertebral Disc Augmentation With Minimally Invasive Surgical Procedure (NCT01442922) | University of Florida | 2011-03-01 |
| Effectiveness of Lumbar Fusion When NanOss Bioactive Is Used With Posterolateral Gutter Fusions (NCT01452516) | Pioneer Surgical Technology, Inc. | 2010-07-01 |
| Clinical Outcomes of Lumbar Degenerative Disc Disease in Active-Duty U.S. Service Personnel (NCT01028300) | Synthes USA HQ, Inc. | 2010-04-01 |
| Treatment of Symptomatic Lumbar Internal Disc Disruption (IDD) With the Biostat® System (NCT01011816) | Spinal Restoration, Inc. | 2010-03-01 |
| A Multicenter, Randomized, Double-blind, Placebo Controlled, Clinical Trial to Evaluate the Safety, Tolerability and Preliminary Effectiveness of 2 Doses of Intradiscal rhGDF-5 (Single Administration) for the Treatment of Early Stage Lumbar Disc Degeneration (NCT01124006) | DePuy Spine | 2010-01-01 |
| An Evaluation of Interlaminar Lumbar Instrumented (ILIF™) (NCT01019057) | NuVasive | 2009-11-01 |
| Efficacy of the Aspen Spinous Process System in Anterior Lumbar Interbody Fusion (ALIF) (NCT01016314) | Zimmer Biomet | 2009-11-01 |
| Trinity Evolution in Posterior or Transforaminal Lumbar Interbody Fusion (PLIF/TLIF) (NCT00965380) | Orthofix Inc. | 2009-09-01 |
| Bone Graft Materials Observational Registry (NCT00974623) | Baxter Healthcare Corporation | 2009-09-01 |
| Safety and Preliminary Efficacy Study of NeoFuse in Subjects Requiring Lumbar Interbody Fusion (NCT00996073) | Mesoblast, Ltd. | 2009-09-01 |
| Trinity Evolution in Anterior Cervical Disectomy and Fusion (ACDF) (NCT00951938) | Orthofix Inc. | 2009-08-01 |
| Actifuse ABX Versus INFUSE in Posterolateral Instrumented Lumbar Fusion (NCT01018771) | Baxter Healthcare Corporation | 2009-07-01 |
| XL TDR® eXtreme Lateral Total Disc Replacement for the Treatment of Lumbar Degenerative Disc Disease (DDD) (NCT00927238) | NuVasive | 2009-07-01 |
| Osteocel® Plus in Posterior Lumbar Interbody Fusion (PLIF) (NCT00941980) | NuVasive | 2009-06-01 |
| Osteocel® Plus in Transforaminal Lumbar Interbody Fusion (TLIF) (NCT00947583) | NuVasive | 2009-05-01 |
| Osteocel® Plus in eXtreme Lateral Interbody Fusion (XLIF®) (NCT00948532) | NuVasive | 2009-03-01 |
| Opioid Treatment for Chronic Low Back Pain and the Impact of Mood Symptoms (NCT01502644) | Brigham and Women's Hospital | 2009-02-01 |
| Trial Evaluating the Safety and Effectiveness of NUBAC™ Disc Arthroplasty (NCT00931515) | Pioneer Surgical Technology, Inc. | 2009-02-01 |
| Maverick Total Disc Replacement in a 'Real World' Patient Population (NCT01338493) | Medtronic Spinal and Biologics | 2009-02-01 |
| Evaluation of Spa Medicine on the Example of Comprehensive Therapy in the Spa Resort Przerzeczyn Zdroj (NCT03405350) | Wroclaw Medical University | 2009-01-01 |
| Pilot Study to Assess Safety/Prelimary Effectiveness of Prefix in Subjects With Degenerative Disc Disease (DDD) Undergoing Spine Fusion Surgery (NCT00798239) | BioSurface Engineering Technologies, Inc | 2008-11-01 |
| Safety and Efficacy Study of NeoFuse in Subjects Requiring Posterolateral Lumbar Fusion (NCT00810212) | Mesoblast, Ltd. | 2008-11-01 |
| Pilot Study to Assess Safety/Preliminary Effectiveness of Prefix in Subjects With Degenerative Disc Disease (DDD) Undergoing Spine Fusion Surgery (NCT00798902) | BioSurface Engineering Technologies, Inc | 2008-11-01 |
| Evaluate Effectiveness of the Biomet Lumbar Spinal Fusion System (NCT00758719) | Zimmer Biomet | 2008-09-01 |
| Intradiscal rhGDF-5 Phase I/II Clinical Trial (NCT00813813) | DePuy Spine | 2008-06-01 |
| Clinical Outcomes of the Trinica(R) Anterior Lumbar Plate: Fixed Screws vs. Variable Screws (NCT00762723) | Zimmer Biomet | 2008-02-01 |
| Study of 3 Doses of NeoFuse Combined With MasterGraft Granules in Subjects Requiring Posterolateral Lumbar Fusion (PLF) (NCT00549913) | Mesoblast, Ltd. | 2007-10-01 |
| INFUSE® Bone Graft/ PEEK Interbody Spacer/ Anterior Cervical Plate Pivotal Clinical Trial (NCT00485173) | Medtronic Spinal and Biologics | 2007-06-01 |
| Actifuse ABX Versus INFUSE in Posterolateral Instrumented Lumbar Fusion (PLIF) With Interbody Fusion (NCT01013389) | Baxter Healthcare Corporation | 2007-06-01 |
| A Pilot Study to Evaluate an Osteogenic Protein 1 (OP-1) Putty Spinal System and an Autograft Spinal System (NCT00678171) | Olympus Biotech Corporation | 2007-02-01 |
| Activ C European Multicenter Study (NCT02492724) | Aesculap AG | 2007-02-01 |
| Activ-L™ Artificial Disc Treatment of Degenerative Disc Disease in the Treatment of Degenerative Disc Disease (NCT00589797) | Aesculap Implant Systems | 2007-01-01 |
| LDR Spine USA Mobi-C(R) Cervical Disc Prosthesis IDE (NCT00389597) | LDR Spine USA | 2006-04-01 |
| Safety and Efficacy Study of Healos as a Bone Replacement to Treat Degenerative Disc Disease (NCT00316121) | Advanced Technologies and Regenerative Medicine, LLC (ATRM) | 2006-04-01 |
| Outcome Study of Patients Treated With Translational Cervical Plate Used to Treat Degenerative Disc Disease (NCT00443547) | Synthes USA HQ, Inc. | 2006-03-01 |
| Evaluation of Radiographic and Patient Outcomes Following Lumbar Spine Fusion Using Demineralized Bone Matrix (DBM) Mixed With Autograft (NCT00254852) | Exactech | 2005-10-01 |
| rhBMP-2/CRM/CD HORIZON® Spinal System Pilot Study (2-Level) (NCT01491568) | Medtronic Spinal and Biologics | 2005-07-01 |
| Advanced MR Imaging in Patients With Painful, Degenerative Disc Disease: A Pilot Study (NCT00706459) | University of California, San Francisco | 2005-03-01 |
| CHARITE™ vs. ALIF 5-Year Follow-up (NCT00215332) | DePuy Spine | 2005-03-01 |
| Kineflex Artificial Disc System to Treat Degenerative Disc Disease (DDD) (NCT00292292) | SpinalMotion | 2005-01-01 |
| Comparison of IDD Therapy and Non-surgical Treatment for Low Back Pain Caused by Degenerative Disc Disease (NCT00165893) | Emory University | 2004-09-01 |
| Disc Prosthesis Versus Multidisciplinary Rehabilitation (NCT00394732) | Ullevaal University Hospital | 2004-04-01 |
| Spine Patient Outcomes Registry for Biomet/EBI (Electro-Biology, Inc) (NCT00726284) | Zimmer Biomet | 2004-04-01 |
| TELAMON P™ Implant/INFUSE® Bone Graft/CD HORIZON® Spinal System Pilot Study (NCT01491516) | Medtronic Spinal and Biologics | 2003-07-01 |
| INFUSE® Bone Graft and MASTERGRAFT® Granules With CD HORIZON® for Posterolateral Lumbar Fusion in Patients With Degenerative Disc Disease - Pilot Study (NCT01491542) | Medtronic Spinal and Biologics | 2003-04-01 |
| Percutaneous Minimal Invasive Pedicular Screw and Rod Insertion in Circumferential Lumbar Fusion (NCT01513577) | Northern Orthopaedic Division, Denmark | 2003-01-01 |
| rhBMP-2/CRM/CD HORIZON® Spinal System Pivotal Study (NCT00707265) | Medtronic Spinal and Biologics | 2002-03-01 |
| Titanium Surgical Mesh and MOSS-Miami Screws for Lumbar Fusion. (NCT00215319) | DePuy Spine | 2000-12-01 |
| Pivotal Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody Fusion in Patients With Symptomatic Degenerative Disc Disease (NCT01494493) | Medtronic Spinal and Biologics | 2000-09-01 |
| CHARITÉ™ Artificial Disc Compared to Anterior Interbody Fusion for Treatment of Degenerative Disc Disease (NCT00215306) | DePuy Spine | 2000-03-01 |
| Clinical Study of rhBMP-2/BCP With the TSRH® Spinal System for Posterolateral Lumbar Fusion in Patients With Degenerative Disc Disease (NCT01494454) | Medtronic Spinal and Biologics | 1999-08-01 |
| Pilot Study of rhBMP/BCP With or Without the TSRH® Spinal System for Posterolateral Lumbar Fusion in Patients With Degenerative Disc Disease (NCT01494441) | Medtronic Spinal and Biologics | 1999-05-01 |
| A Pivotal Study of rhBMP-2/ACS/INTER FIX™ Device for Posterior Lumbar Interbody Fusion in Patients With Degenerative Disc Disease (NCT01491464) | Medtronic Spinal and Biologics | 1999-03-01 |
| A Pilot Study of rhBMP-2/ACS With the INTERFIX™ Device for the AnteriorLumbar Interbody Fusion in Patients With Degenerative Disc Disease (NCT01491451) | Medtronic Spinal and Biologics | 1999-02-01 |
| A Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fusion in Patients With Degenerative Disc Disease (NCT01491425) | Medtronic Spinal and Biologics | 1998-11-01 |
| Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate System (NCT00726128) | Zimmer Biomet | 1998-08-01 |
| Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fusion in Patients With Symptomatic Degenerative Disc Disease (NCT01491386) | Medtronic Spinal and Biologics | 1998-08-01 |
| A Pilot Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody Fusion in Patients With Symptomatic Degenerative Disc Disease (NCT01494428) | Medtronic Spinal and Biologics | 1998-04-01 |
| Pilot Study of rhBMP-2/BCP in Patients With Spinal Degeneration With Instability Requiring Surgical Fusion (NCT01495234) | Medtronic Spinal and Biologics | 1996-10-01 |