| Gabapentin Versus Transdermal Fentanyl Matrix for Chronic Neuropathic Pain (NCT01127100) | Seoul National University Hospital | 2010-05-01 |
| Prospective Study of Minimally Invasive Spine Surgery (NCT01045473) | Society for Minimally Invasive Spine Surgery | 2010-01-01 |
| Neurogenic Intermittent Claudication Evaluation Study (NCT00905359) | Medtronic Spinal and Biologics | 2010-01-01 |
| 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 |
| Intraoperative Infusion of Precedex to Reduce Length of Stay After Lumbar Spine Fusion (NCT00808665) | Vanderbilt University Medical Center | 2009-06-01 |
| Efficacy of Pregabalin in Patients With Radicular Pain (NCT00908375) | Northwestern University | 2009-05-01 |
| Safety and Efficacy Study of NeoFuse in Subjects Requiring Posterolateral Lumbar Fusion (NCT00810212) | Mesoblast, Ltd. | 2008-11-01 |
| A Study of the In-Space Device for Treatment of Moderate Spinal Stenosis (NCT00697827) | Synthes USA HQ, Inc. | 2008-06-01 |
| Clinical Outcomes of the Trinica(R) Anterior Lumbar Plate: Fixed Screws vs. Variable Screws (NCT00762723) | Zimmer Biomet | 2008-02-01 |
| Clinical Trial Comparing Decompression With and Without Coflex™ Interlaminar Technology Treating Lumbar Spinal Stenosis (NCT01316211) | Paradigm Spine | 2008-01-01 |
| Study of 3 Doses of NeoFuse Combined With MasterGraft Granules in Subjects Requiring Posterolateral Lumbar Fusion (PLF) (NCT00549913) | Mesoblast, Ltd. | 2007-10-01 |
| Spine Research With Roentgen Stereophotogrammetric Analysis (NCT00493558) | Nova Scotia Health Authority | 2007-07-01 |
| Spine Fusion Instrumented With BMP-2 vs Uninstrumented With Infuse BMP-2 Alone (NCT00405600) | Nova Scotia Health Authority | 2006-11-01 |
| Intermittent Neurogenic Claudication Treatment With APERIUS® (NCT00887744) | Medtronic Spinal and Biologics | 2006-11-01 |
| Total Facet Arthroplasty System®(TFAS®) Clinical Trial (NCT00418197) | Archus Orthopedics, Inc. | 2005-08-01 |
| Lumbar Interbody Fusion Using the Telamon® Peek™ Versus the Telamon® Hydrosorb™ Fusion Device (NCT00095095) | Medtronic Spinal and Biologics | 2004-10-01 |
| Spine Patient Outcomes Registry for Biomet/EBI (Electro-Biology, Inc) (NCT00726284) | Zimmer Biomet | 2004-04-01 |
| A Clinical Study of the Dynesys(R) Spinal System (NCT00759057) | Zimmer Biomet | 2003-03-01 |
| Greenwich Lumbar Stenosis SLIP Study (NCT00109213) | Greenwich Hospital | 2002-05-01 |
| Surgical Versus Nonsurgical Treatment for Spinal Stenosis (NCT00022776) | University of Pittsburgh | 2000-09-01 |
| Epsilon-Aminocaproaic Acid to Reduce the Need for Blood Transfusions During and Following Spine Surgery (NCT00320619) | National Heart, Lung, and Blood Institute (NHLBI) | 2000-09-01 |
| Spine Patient Outcomes Research Trial (SPORT): Spinal Stenosis (NCT00000411) | Dartmouth-Hitchcock Medical Center | 2000-03-01 |
| Spine Patient Outcomes Research Trial (SPORT): Degenerative Spondylolisthesis With Spinal Stenosis (NCT00000409) | Dartmouth-Hitchcock Medical Center | 2000-03-01 |