Patient Outcomes Using an Expandable Spacer
NCT03162666 · Status: WITHDRAWN · Type: OBSERVATIONAL
Last updated 2021-08-23
Summary
This study is a post-market clinical follow-up study. The data collected from this study will serve the purpose of confirming safety and performance of the ALTERA™ Expandable implant.
Conditions
- Degenerative Disc Disease
Interventions
- DEVICE
-
ALTERA
degenerative disc disease (DDD) at one or two contiguous levels from L2 to S1. with up to grade 1 spondylolisthesis
Sponsors & Collaborators
-
Globus Medical Inc
lead INDUSTRY
Principal Investigators
-
Kern Singh, MD · Rush Univeristy Medical Center Orthopedic Surgeon
Eligibility
- Min Age
- 18 Years
- Max Age
- 70 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2017-02-28
- Primary Completion
- 2020-11-06
- Completion
- 2020-11-06
- FDA Device
- Yes
Countries
- United States
Study Locations
More Related Trials
-
Pilot Study of rhBMP/BCP With or Without the TSRH® Spinal System for Posterolateral Lumbar Fusion in Patients With Degenerative Disc Disease
NCT01494441 ·Status: COMPLETED ·Phase: NA
-
A Pilot Study of rhBMP-2/ACS/Allograft Bone Dowel for Anterior Lumbar Interbody Fusion in Patients With Symptomatic Degenerative Disc Disease
NCT01494428 ·Status: COMPLETED ·Phase: NA
-
FIBERGRAFT Aeridyan Posterolateral Fusion Study
NCT07059065 ·Status: RECRUITING ·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
-
Post Marketing Study of MagnetOs Easypack Putty Standalone Compared to Demineralized Bone Matrix or Fibers Mixed With Autograft in Patients Undergoing Posterolateral Lumbar Fusion
NCT04679844 ·Status: RECRUITING ·Phase: NA
-
Bone Graft Materials Observational Registry
NCT00974623 ·Status: TERMINATED
-
A Retrospective Study Using CALIBER® TLIF Expandable Spacer in the Treatment of DDD: 2 Year Follow-up.
NCT02388022 ·Status: COMPLETED
-
Comparison of the Aspen Device Versus Pedicle Screws for Supplemental Posterior Fixation in Lumbar Interbody Fusion
NCT01549366 ·Status: COMPLETED ·Phase: NA
-
Evaluation of Radiographic and Patient Outcomes Following Lumbar Spine Fusion Using Demineralized Bone Matrix (DBM) Mixed With Autograft
NCT00254852 ·Status: TERMINATED ·Phase: NA
-
Comparison of Radiographic Fusion Rate and Clinical Outcome of ALIF and XLIF Performed With Either Recombinant Human Bone Morphogenetic Protein-2 or ViviGen®
NCT05238740 ·Status: RECRUITING ·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
-
Clinical Outcome and Fusion Rate of 3D Printed Interbody Fusion Cages and Titanium Coated PEEK Cages
NCT05237908 ·Status: ACTIVE_NOT_RECRUITING
-
A Prospective Analysis of the Efficacy of Allosync Expand and Autograft Bone Graft in Open Lumbar Spinal Fusion
NCT06415110 ·Status: ENROLLING_BY_INVITATION
-
Impact of Local Steroid Application in Extreme Lateral Lumbar Interbody Fusion
NCT03327272 ·Status: WITHDRAWN ·Phase: PHASE3
-
Post-market Surveillance Study of FLXfit™ TLIF Interbody Fusion Device
NCT02805985 ·Status: UNKNOWN ·Phase: NA
-
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
-
LDGraft in Single Level Anterior Lumbar Interbody Fusion (ALIF)
NCT06462729 ·Status: RECRUITING ·Phase: PHASE1/PHASE2
-
Study of an Expandable Interbody Device for the Lumbar Spine
NCT02075554 ·Status: COMPLETED ·Phase: NA
-
Performance of Inductigraft in Spinal Fusion
NCT01452022 ·Status: COMPLETED ·Phase: NA
-
Supplemental Anterior Lumbar Interbody Fusion (ALIF) in Spinal Deformity
NCT01601054 ·Status: COMPLETED ·Phase: NA
-
Study Evaluating the Safety and Effectiveness of the FLEXUS(TM) Interspinous Spacer
NCT01156675 ·Status: TERMINATED ·Phase: NA
-
Prospective Post-market Clinical Follow-up Study of the HBS 2 Resorb Mg in Patients With Intra- and Extraarticular Fractures, Pseudarthroses and Arthrodesis of Small Bones and Bone Fragments.
NCT05483387 ·Status: RECRUITING ·Phase: PHASE4
-
Intervertebral Disc Augmentation With Minimally Invasive Surgical Procedure
NCT01442922 ·Status: COMPLETED
-
INFUSE® Bone Graft and MASTERGRAFT® Granules With CD HORIZON® for Posterolateral Lumbar Fusion in Patients With Degenerative Disc Disease - Pilot Study
NCT01491542 ·Status: COMPLETED ·Phase: NA
-
Sterile Amniotic Fluid Filtrate Epidural Injection.
NCT04537026 ·Status: COMPLETED ·Phase: PHASE1/PHASE2