Post-Marketing Clinical Follow-Up of a Spine Implant

Postmarket Clinical Follow-Up Study on Arcadius XP L® Interbody Fusion Device

NCT05944081 ·Status: WITHDRAWN

Freedom Lumbar Disc in the Treatment of Lumbar Degenerative Disc Disease

NCT00775801 ·Status: UNKNOWN ·Phase: NA

Safety and Preliminary Effectiveness of NVD-001 for the Treatment of Low Grade Degenerative Lumbar Spondylolisthesis

NCT03100032 ·Status: COMPLETED ·Phase: PHASE1/PHASE2

Safety and Performance Study of the CAdiscTM-L Lumbar Spinal Disc Replacement Device For CE Marking

NCT00949936 ·Status: COMPLETED ·Phase: NA

Clinical and Radiological Evaluation of Patients With DDD Following TLIF With 3-D Printed Titanium Cage

NCT03018392 ·Status: COMPLETED ·Phase: NA

A Comparison of Stryker's Tritanium Posterior Lumbar Cage and PEEK Implant

NCT03817606 ·Status: TERMINATED ·Phase: NA

Retrospective/Prospective Data Collection on the LDR ROIC Interbody Fusion Device With VerteBRIDGE Plating

NCT02104167 ·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

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

Retrospective/Prospective Data Collection on the LDR ROIA Interbody Fusion Device With VerteBRIDGE Plating

NCT02104141 ·Status: COMPLETED

ArcadiusXP L Post Market Clinical Follow-Up

NCT01895426 ·Status: COMPLETED

Treatment of Symptomatic Lumbar Internal Disc Disruption (IDD) With the Biostat® Disc Augmentation System: A Pilot Study

NCT00693784 ·Status: COMPLETED ·Phase: NA

Incidence of Large Annular Defects in Primary Lumbar Discectomy Patients

NCT03252691 ·Status: WITHDRAWN

Lumbar Discopathy Decompression with Lateral Interbody Fusion: Radiological and Clinical Outcomes

NCT06719349 ·Status: COMPLETED

Freedom® Cervical Disc Use In The Treatment of Cervical Degenerative Disc Disease

NCT01763619 ·Status: UNKNOWN ·Phase: NA

Pivotal Study of rhBMP-2/ACS/LT-CAGE® Device for Anterior Lumbar Interbody Fusion in Patients With Symptomatic Degenerative Disc Disease

NCT01491386 ·Status: COMPLETED ·Phase: NA

A Comparative Study Between Mechanical and a Viscoelastic Disc Prosthesis in the Lumbar Spine

NCT03716947 ·Status: UNKNOWN ·Phase: NA

Study of the Safety and Effectiveness of the Artificial Cervical Disc - Low Profile Device at Two Adjacent Levels

NCT00637156 ·Status: COMPLETED ·Phase: NA

Study With NVDX3 for Treatment of Low Grade Degenerative Lumbar Spondylolisthesis

NCT05961956 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE1/PHASE2

Titanium vs. PEEK Fusion Devices in 1 Level TLIF

NCT05691062 ·Status: ENROLLING_BY_INVITATION ·Phase: PHASE4

The Ailliance Post-Market Clinical Study

NCT05856370 ·Status: RECRUITING ·Phase: NA

Efficacy and Safety of IntraSPINE® Associated with Discectomy in the Treatment of Lumbar Disc Herniation.

NCT03752671 ·Status: COMPLETED ·Phase: NA

Pivotal Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody Fusion in Patients With Symptomatic Degenerative Disc Disease

NCT01494493 ·Status: TERMINATED ·Phase: NA

Vertebral Augmentation Using VCFix Spinal System in Stand-alone Configuration

NCT07259811 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA

Clinical Trial Comparing Decompression With and Without Coflex™ Interlaminar Technology Treating Lumbar Spinal Stenosis

NCT01316211 ·Status: COMPLETED ·Phase: NA