Globus Medical: all 71 studies
Page 1 of 1. Open to participants first (10), then studies with results posted, then the rest; newest registration first within each.
- A Retrospective Review: Outcomes of the REFLECT™ System for Idiopathic ScoliosisNot yet recruitingNCT07589023
- A Study of Precice Intramedullary Limb Lengthening System (IMLL) Limb Lengthening ProceduresEnrolling by invitationNCT06741514
- A Review of Precice Intramedullary Limb Lengthening (IMLL) System for Limb Lengthening Procedures in Children.Enrolling by invitationNCT06714110
- REFLECT Scoliosis System Post Approval StudyRecruitingNCT06298812Not applicable
- Long-Term Assessment of the Safety and Performance of the NuVasive Simplify Disc at Two LevelsEnrolling by invitationNCT05691231
- NuVasive® ACP System StudyEnrolling by invitationNCT05066711
- Posterior Cervical Fixation StudyEnrolling by invitationNCT04770571
- Cervical Interbody Implant StudyEnrolling by invitationNCT04689854
- Lumbar Interbody Implant StudyEnrolling by invitationNCT04418830
- Advanced Materials Science in XLIF StudyEnrolling by invitationNCT03649490
- Post Approval Study Protocol for the Two Level Simplify® Cervical Artificial DiscCompletedNCT04980378Results posted
- Post-Approval Study Protocol for the Simplify Cervical Artificial DiscCompletedNCT04630626Not applicableResults posted
- Comparison of 10 kHz SCS Combined With CMM to CMM Alone in the Treatment of Neuropathic Limb PainCompletedNCT03228420Not applicableResults posted
- Investigation of the Two Level Simplify® Cervical Artificial DiscCompletedNCT03123549Not applicableResults posted
- Investigation of the Simplify® Cervical Artificial DiscCompletedNCT02667067Not applicableResults posted
- A Prospective Randomized Postmarket Clinical Study of the TRANSITION Stabilization SystemTerminatedNCT02184520Not applicableResults posted
- Study of an Expandable Interbody Device for the Lumbar SpineCompletedNCT02075554Not applicableResults posted
- TRIUMPH Lumbar Artificial Disc IDE: A Pilot StudyCompletedNCT01198470Not applicableResults posted
- Study Evaluating the Safety and Effectiveness of the FLEXUS(TM) Interspinous SpacerTerminatedNCT01156675Not applicableResults posted
- SECURE®-C Cervical Artificial Disc Clinical Study/ SECURE-C Cervical Artificial Disc Postmarket Approval StudyCompletedNCT00882661Not applicableResults posted
- PCM Cervical Disc SystemCompletedNCT00578812Phase 3Results posted
- A Pivotal Study of a Facet Replacement System to Treat Spinal StenosisCompletedNCT00401518Not applicableResults posted
- Sacroiliac (SI) Joint Transfixing and Fusion: Meaningful Long Term Outcomes With Nevro1CompletedNCT06909292
- Clinical Trial of MED HF10™ Spinal Cord Stimulation for the Treatment of Chronic PainActive, not recruitingNCT06897280Phase 4
- Pain and Neurological Function Improvements With 10 kHz Spinal Cord Stimulation Treatment of Painful Diabetic NeuropathyActive, not recruitingNCT05777317Not applicable
- Retrospective Modulus ALIF StudyCompletedNCT05566704
- PDN Post Market, Multicenter, Prospective, Global Clinical StudyActive, not recruitingNCT05301816Not applicable
- Long-term Assessment of the Safety and Performance of the NuVasive Simplify DiscActive, not recruitingNCT05258435
- XLIF Decade Plate System StudyCompletedNCT04689880
- MSK Validation StudyCompletedNCT04422288
- MLX/XLX ACR Expandable Lumbar Interbody ImplantsCompletedNCT04420143
- Modulus in XLIF StudyCompletedNCT04418817
- Prospective Robotic Global Research Study (PROGRESS)Status unknownNCT04257279Not applicable
- Amnios™ RT Outcomes StudyCompletedNCT04088383Not applicable
- HF10 Treatment of Chronic Knee PainTerminatedNCT04020211
- Comparison of HF10 Therapy Combined With CMM to CMM Alone in the Treatment of Non-Surgical Refractory Back PainCompletedNCT03680846Not applicable
- Computerized Tomography (CT) Scan Study of Bone Healing Following Open Wedge Proximal Tibial OsteotomyCompletedNCT03431662Not applicable
- Preliminary Investigation of ViaShield™ Amnion Patch as an Anti-Adhesive Barrier in HemicraniectomiesWithdrawnNCT03371316Not applicable
- Patient Outcomes Using an Expandable SpacerWithdrawnNCT03162666
- SCS for the Treatment Of Chronic Pain of the Upper ExtremitiesCompletedNCT02703818Not applicable
- Comprehensive Spinal Alignment Planning StudyCompletedNCT02606695
- Ellipse Intramedullary High Tibial Osteotomy Nail StudyCompletedNCT02519218
- Ellipse Intramedullary Nail High Tibial Osteotomy StudyCompletedNCT02412163
- A Retrospective Study Using CALIBER® TLIF Expandable Spacer in the Treatment of DDD: 2 Year Follow-up.CompletedNCT02388022
- Clinical Trial of the Senza™ SCS System in the Treatment of Chronic Upper Limb and Neck PainCompletedNCT02385201Not applicable
- INDEPENDENCE Spacer for Lumbar FusionCompletedNCT02299323
- Advanced XLIF Monitoring Multicenter StudyCompletedNCT02272140
- AttraX® Putty vs. Autograft in XLIF®CompletedNCT02250248Not applicable
- Advanced XLIF Monitoring Pilot StudyCompletedNCT02192112
- Post-Approval Clinical Trial of the PCM® Cervical DiscCompletedNCT01905930Phase 3
- Treatment of Sacroiliac Dysfunction With SI-LOK® Sacroiliac Joint Fixation SI-SI-LOKCompletedNCT01861899
- A Retrospective Review of Early Onset Spinal Deformity Patients Treated With the Ellipse MAGEC SystemCompletedNCT01716936
- A Prospective Non-concurrent Controlled Evaluation of Open and MAS® PLIFCompletedNCT01640977
- Treatment of Adolescent Idiopathic Scoliosis Patients Using the Ellipse MAGEC SystemStatus unknownNCT01633931
- Comparison of Senza to Commercial Spinal Cord Stimulation for the Treatment of Chronic PainStatus unknownNCT01609972Not applicable
- Post-Market Study of the Ellipse PRECICE Intramedullary Limb Lengthening SystemStatus unknownNCT01601301Not applicable
- Multimodality Neuromonitoring in XLIFCompletedNCT01499680
- Proximal Junctional Kyphosis Following Long Instrumented Spinal Fusion: The Effect of Implant SelectionWithdrawnNCT01441999Not applicable
- A Clinical Trial Evaluating a Total Disc Replacement in Patients With Cervical Disc DiseaseTerminatedNCT01433367
- SpineTRACK Registry - Spinal Outcomes RegistryCompletedNCT01372592
- Study of the Surgical Treatment of Early Onset Scoliosis Using a Non-invasive Growing RodCompletedNCT01362881
- NeuroVision® Dynamic Screw Test StudyCompletedNCT01232517
- XLIF® vs. MAS®TLIF for the Treatment of Symptomatic Lumbar Degenerative Spondylolisthesis With or Without Central Stenosis.CompletedNCT01024699
- An Evaluation of Interlaminar Lumbar Instrumented (ILIF™)CompletedNCT01019057
- 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 Anterior Cervical Discectomy and Fusion (ACDF)CompletedNCT00942045
- 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
- Evaluating The Safety and Effectiveness of The NeoDisc™ Versus ACDF in Subjects With Single-Level Cervical Disc DiseaseCompletedNCT00478088Not applicable