Post-marketing Clinical Follow-up of the Medical Device DIVA®

A Questionnaire Survey Study for Exploring Outcomes for Patients With Disc Herniation

NCT05752838 ·Status: COMPLETED

CARES Lumbar Artificial Disc Registry

NCT02139527 ·Status: TERMINATED

DIAM™ Spinal Stabilization System Long Term Follow up Clinical Plan

NCT05201573 ·Status: UNKNOWN

Effectiveness of Lumbar Traction in Lumbar Disk Herniation

NCT02793440 ·Status: UNKNOWN ·Phase: NA

Study of the Safety and Effectiveness of DIAM™ Spinal Stabilization System Versus Conservative Care

NCT00456378 ·Status: TERMINATED ·Phase: NA

Retrospective Multicenter Clinical Evaluation of Complications for Single or Multilevel VEO® Lateral Access and Interbody Fusion System and eXtreme Lateral Interbody Fusion (XLIF®) Subjects

NCT01878149 ·Status: COMPLETED

Safety and Performance of a Hernia Blocking System

NCT04188236 ·Status: COMPLETED ·Phase: NA

Correlation Between RMI of Degenerative Disk Disease and Reduction of Pain After Disk-infiltration Treatments

NCT04142580 ·Status: COMPLETED

A Multi-Center, Prospective Historically Controlled Clinical Trial Comparing the Safety and Effectiveness of Triadyme-C to a Total Disc Replacement Control Cohort in the Treatment of Symptomatic Cervical Disc Disease (SCDD) at a Single Level

NCT07287449 ·Status: NOT_YET_RECRUITING ·Phase: NA

Lumbar Degenerative Disc Disease Treatment With Bone Marrow Autologous Mesenchymal Stem Cells (MSV)

NCT02440074 ·Status: WITHDRAWN ·Phase: PHASE1/PHASE2

LISA Post Market Clinical Follow-Up Study: Documentation of Clinical Outcomes After Surgery With LISA Implant

NCT04631133 ·Status: RECRUITING

Maverick Total Disc Replacement in a 'Real World' Patient Population

NCT01338493 ·Status: COMPLETED

Retrospective Chart Review to Assess Outcomes in Subjects That Received MAGNIFUSE® in the Posterolateral Lumbar Spine

NCT02684045 ·Status: COMPLETED

Full-Endoscopic vs Open Discectomy for the Treatment of Symptomatic Lumbar Herniated Disc

NCT02441959 ·Status: TERMINATED ·Phase: NA

Efficacy of Navigable Percutaneous Plasma Disc Decompression Device (L'DISQ) in Patients With Severe Lumbar Disc Herniation

NCT05231759 ·Status: UNKNOWN

DIAM™ Spinal Stabilization System vs. Decompression, Formerly vs. Posterolateral Fusion

NCT00627497 ·Status: TERMINATED ·Phase: PHASE3

Long-term Assessment of the Safety and Performance of the NuVasive Simplify Disc

NCT05258435 ·Status: ACTIVE_NOT_RECRUITING

Detection of Bacteria in Herniated Nucleus Material in Lumbar Disc Herniations by Culture and PCR

NCT02385968 ·Status: TERMINATED

Return to Work After Early Intervention for Lumbar Disc Herniation Versus Usual Care

NCT04657354 ·Status: WITHDRAWN ·Phase: NA

Learning Curve, Outcome Parameters, and MRI Assessment of Disc Evacuation After Transforaminal Percutaneous Endoscopic Lumbar Discectomy

NCT05521750 ·Status: COMPLETED

Clinical Outcome Study of Minimally Invasive Decompression for Lumbar Spinal Stenosis

NCT00737607 ·Status: UNKNOWN

Advanced XLIF Monitoring Multicenter Study

NCT02272140 ·Status: COMPLETED

Preoperative Estimation Of Disc Herniation Recurrence In Patients With Lumbar Disc Herniation

NCT04254250 ·Status: COMPLETED

A Pivotal Study of rhBMP-2/ACS/INTER FIX™ Device for Posterior Lumbar Interbody Fusion in Patients With Degenerative Disc Disease

NCT01491464 ·Status: TERMINATED ·Phase: NA

Outcome Analysis for Minimally Invasive Spine Surgery and Navigation

NCT01751841 ·Status: COMPLETED