Intervertebral Disc Degeneration: all 472 studies
Page 5 of 5. Open to participants first (100), then studies with results posted, then the rest; newest registration first within each.
- Pilot Study of rhBMP-2/BCP in Patients With Spinal Degeneration With Instability Requiring Surgical FusionCompletedNCT01495234Not applicable
- Pivotal Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody Fusion in Patients With Symptomatic Degenerative Disc DiseaseTerminatedNCT01494493Not applicable
- Clinical Study of rhBMP-2/BCP With the TSRH® Spinal System for Posterolateral Lumbar Fusion in Patients With Degenerative Disc DiseaseCompletedNCT01494454Not applicable
- Pilot Study of rhBMP/BCP With or Without the TSRH® Spinal System for Posterolateral Lumbar Fusion in Patients With Degenerative Disc DiseaseCompletedNCT01494441Not applicable
- A Pilot Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody Fusion in Patients With Symptomatic Degenerative Disc DiseaseCompletedNCT01494428Not applicable
- rhBMP-2/CRM/CD HORIZON® Spinal System Pilot Study (2-Level)CompletedNCT01491568Not applicable
- INFUSE® Bone Graft and MASTERGRAFT® Granules With CD HORIZON® for Posterolateral Lumbar Fusion in Patients With Degenerative Disc Disease - Pilot StudyCompletedNCT01491542Not applicable
- TELAMON P™ Implant/INFUSE® Bone Graft/CD HORIZON® Spinal System Pilot StudyCompletedNCT01491516Not applicable
- INFUSE ® Bone Graft/CORNERSTONE-SR® Allograft Ring/ATLANTIS® Anterior Cervical Plate System Pivotal TrialTerminatedNCT01491477Not applicable
- A Pivotal Study of rhBMP-2/ACS/INTER FIX™ Device for Posterior Lumbar Interbody Fusion in Patients With Degenerative Disc DiseaseTerminatedNCT01491464Not applicable
- A Pilot Study of rhBMP-2/ACS With the INTERFIX™ Device for the AnteriorLumbar Interbody Fusion in Patients With Degenerative Disc DiseaseCompletedNCT01491451Not applicable
- A Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fusion in Patients With Degenerative Disc DiseaseCompletedNCT01491425Not applicable
- INFUSE™ BONE GRAFT/CORNERSTONE-SR™ Allograft Ring/ATLANTIS™ Anterior Cervical Plate- Pilot StudyCompletedNCT01491399Not applicable
- Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fusion in Patients With Symptomatic Degenerative Disc DiseaseCompletedNCT01491386Not applicable
- Pilot Study of rhBMP-2/ACS/LT-CAGE® for Anterior Lumbar Interbody Fusion in Patients With Degenerative Disc DiseaseCompletedNCT01491373Not applicable
- Minuteman Spinal Fusion Implant Versus Surgical Decompression for Lumbar Spinal StenosisCompletedNCT01455805Not applicable
- Effectiveness of Lumbar Fusion When NanOss Bioactive Is Used With Posterolateral Gutter FusionsTerminatedNCT01452516Not applicable
- Performance of Inductigraft in Spinal FusionCompletedNCT01452022Not applicable
- Intervertebral Disc Augmentation With Minimally Invasive Surgical ProcedureCompletedNCT01442922
- Study of Bioactive Glass-ceramic Intervertebral Spacer (Bonglass-SS) in Posterior Lumbar Interbody FusionStatus unknownNCT01439464Not applicable
- PEEK and Allograft Spacers Evaluation in Spinal Fusion SurgeriesCompletedNCT01406405
- Dynamic Stabilization Versus FusionCompletedNCT01365754Not applicable
- Patient Positioning in Lumbar Fusion Surgery and Its Impact on Spinal Sagittal Balance and Surgeon SatisfactionTerminatedNCT01326091Not applicable
- Radiographic and Clinical Outcomes of PureGen in Posterior Lumbar (PLIF) and Transforaminal Interbody Fusion (TLIF)TerminatedNCT01293981
- PureGen: Radiographic Analysis of Fusion for ACDFTerminatedNCT01291134
- Safety and Preliminary Efficacy Study of Mesenchymal Precursor Cells (MPCs) in Subjects With Lumbar Back PainCompletedNCT01290367Phase 2
- Isolation and Authentication of Mesenchymal Stem Cell-like Progenitor Cells From the Degenerated Intervertebral Disc of Lumbar SpineStatus unknownNCT01213953
- Safety and Efficacy Study of NeoFuse in Subjects Undergoing Multi-Level Anterior Cervical Discectomy and FusionCompletedNCT01106417Phase 1/2
- Safety and Preliminary Efficacy Study of NeoFuse in Subjects Undergoing Multi-Level Anterior Cervical DiscectomyCompletedNCT01097486Phase 2
- Prospective Study of Minimally Invasive Spine SurgeryStatus unknownNCT01045473
- An Evaluation of Interlaminar Lumbar Instrumented (ILIF™)CompletedNCT01019057
- Actifuse ABX Versus INFUSE in Posterolateral Instrumented Lumbar FusionCompletedNCT01018771Not applicable
- Efficacy of the Aspen Spinous Process System in Anterior Lumbar Interbody Fusion (ALIF)WithdrawnNCT01016314Not applicable
- Actifuse ABX Versus INFUSE in Posterolateral Instrumented Lumbar Fusion (PLIF) With Interbody FusionCompletedNCT01013389Not applicable
- Comparison of Cage Versus Plate in One Level Cervical Disc DiseaseCompletedNCT01011569
- Safety and Preliminary Efficacy Study of NeoFuse in Subjects Requiring Lumbar Interbody FusionCompletedNCT00996073Phase 2
- Bone Graft Materials Observational RegistryTerminatedNCT00974623
- Trinity Evolution in Posterior or Transforaminal Lumbar Interbody Fusion (PLIF/TLIF)CompletedNCT00965380
- Trinity Evolution in Anterior Cervical Disectomy and Fusion (ACDF)CompletedNCT00951938
- Safety and Performance Study of the CAdiscTM-L Lumbar Spinal Disc Replacement Device For CE MarkingCompletedNCT00949936Not applicable
- Osteocel® Plus in Anterior Lumbar Interbody Fusion (ALIF)CompletedNCT00948831
- Osteocel® Plus in eXtreme Lateral Interbody Fusion (XLIF®)CompletedNCT00948532
- Osteocel® Plus in Transforaminal Lumbar Interbody Fusion (TLIF)CompletedNCT00947583
- Osteocel® Plus in Posterior Lumbar Interbody Fusion (PLIF)CompletedNCT00941980
- XL TDR® eXtreme Lateral Total Disc Replacement for the Treatment of Lumbar Degenerative Disc Disease (DDD)CompletedNCT00927238Phase 3
- Percutaneous Dynamic Stabilization (PDS) System Versus Fusion for Treating Degenerative Disc DiseaseTerminatedNCT00878579Phase 2
- Safety and Efficacy Study of NeoFuse in Subjects Requiring Posterolateral Lumbar FusionWithdrawnNCT00810212Phase 1/2
- Pilot Study to Assess Safety/Preliminary Effectiveness of Prefix in Subjects With Degenerative Disc Disease (DDD) Undergoing Spine Fusion SurgeryStatus unknownNCT00798902Phase 1/2
- Pilot Study to Assess Safety/Prelimary Effectiveness of Prefix in Subjects With Degenerative Disc Disease (DDD) Undergoing Spine Fusion SurgeryStatus unknownNCT00798239Phase 1/2
- Freedom Lumbar Disc in the Treatment of Lumbar Degenerative Disc DiseaseStatus unknownNCT00775801Not applicable
- Evaluate Effectiveness of the Biomet Lumbar Spinal Fusion SystemCompletedNCT00758719
- Fusion Assessment Clinical TrialCompletedNCT00736398
- Evaluation Of Spinelink® Fixation In The Treatment Of Degenerative Spondylolisthesis And Spinal InstabilityCompletedNCT00726310
- Spine Patient Outcomes Registry for Biomet/EBI (Electro-Biology, Inc)CompletedNCT00726284
- Patient Outcomes Evaluation of the EBI Vuelock™ Anterior Cervical Plate SystemCompletedNCT00726128
- rhBMP-2/CRM/CD HORIZON® Spinal System Pivotal StudyCompletedNCT00707265Phase 3
- Advanced MR Imaging in Patients With Painful, Degenerative Disc Disease: A Pilot StudyTerminatedNCT00706459
- A Pilot Study to Evaluate an Osteogenic Protein 1 (OP-1) Putty Spinal System and an Autograft Spinal SystemCompletedNCT00678171Not applicable
- PRESTIGE® Cervical Disc StudyCompletedNCT00642876Not applicable
- Evaluation of the Prosthetic Disc ReplacementTerminatedNCT00640029Not applicable
- Study of 3 Doses of NeoFuse Combined With MasterGraft Granules in Subjects Requiring Posterolateral Lumbar Fusion (PLF)CompletedNCT00549913Phase 1/2
- Study of the Safety and Effectiveness of DIAM™ Spinal Stabilization System Versus Conservative CareTerminatedNCT00456378Not applicable
- Pivotal IDE Study of the BRYAN(R) Cervical Disc Prosthesis in the Treatment of DDD Versus ACDFCompletedNCT00437190Not applicable
- Disc Prosthesis Versus Multidisciplinary RehabilitationCompletedNCT00394732Not applicable
- Kineflex|C Artificial Disc System to Treat Cervical Degenerative Disc Disease (DDD)TerminatedNCT00374413Not applicable
- Kineflex Artificial Disc System to Treat Degenerative Disc Disease (DDD)TerminatedNCT00292292Not applicable
- Evaluation of Radiographic and Patient Outcomes Following Lumbar Spine Fusion Using Demineralized Bone Matrix (DBM) Mixed With AutograftTerminatedNCT00254852Not applicable
- CHARITE™ vs. ALIF 5-Year Follow-upCompletedNCT00215332
- Titanium Surgical Mesh and MOSS-Miami Screws for Lumbar Fusion.CompletedNCT00215319Phase 3
- CHARITÉ™ Artificial Disc Compared to Anterior Interbody Fusion for Treatment of Degenerative Disc DiseaseCompletedNCT00215306Phase 3
- Cervical I/F Cage for Anterior Cervical FusionCompletedNCT00215293Phase 3
- Comparison of IDD Therapy and Non-surgical Treatment for Low Back Pain Caused by Degenerative Disc DiseaseCompletedNCT00165893Phase 4