GO-LIF With Percutaneous Facet Fusion
NCT01269398 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL
Last updated 2013-03-22
Summary
Utilization of trans-pedicular trans-discal implants for stabilization of a single lumbar motion segment, in conjunction with posterior facets fusion. The trajectories are planned and achieved by means of the SpineAssist® system - a computerized, image-based guidance system that assists surgeons in precisely guiding spinal surgical tools and implants in line with a CT-based pre-operative plan. GO-LIF and SpineAssist are CE marked products.
Thy study's objective is to to collect data regarding the ability to achieve solide fusion, comibing the GO-LIF procedure for spinal fixation and stabilization with percutaneous posterior facets fusion.
Conditions
- Lumbar Fusion
Interventions
- DEVICE
-
GO-LIF and SpineAssist SYSTEMS
Sponsors & Collaborators
-
Hadassah Medical Organization
lead OTHER
Study Design
- Allocation
- NA
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 80 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Primary Completion
- 2014-08-31
Countries
- Israel
Study Locations
More Related Trials
-
New Robotic Assistance System for Spinal Fusion Surgery
NCT02558621 ·Status: COMPLETED ·Phase: NA
-
A Feasibility Study to Evaluate the TURRIS Facet Fusion System in Lumbar Spinal Surgery
NCT02294669 ·Status: TERMINATED ·Phase: NA
-
Lumbar & Sacroiliac Fusion Study Involving Previously Implanted Devices
NCT07204288 ·Status: RECRUITING ·Phase: NA
-
SI Joint Stabilization in Long Fusion to the Pelvis
NCT04062630 ·Status: COMPLETED ·Phase: NA
-
Assessment of nanOss Bioactive 3D in the Posterolateral Spine
NCT01829997 ·Status: COMPLETED ·Phase: NA
-
Effectiveness of Lumbar Fusion When NanOss Bioactive Is Used With Posterolateral Gutter Fusions
NCT01452516 ·Status: TERMINATED ·Phase: NA
-
Efficacy of Hybrid Systems in Comparison to the Rigid Spondylodesis in Lumbar-spine Fusion
NCT01852526 ·Status: TERMINATED ·Phase: NA
-
Percutaneous Trans-facet Spine Fixation
NCT07001969 ·Status: ENROLLING_BY_INVITATION ·Phase: NA
-
OLIF25™ /OLIF51™ Study
NCT02657421 ·Status: TERMINATED
-
SPONGIT: Comparison of Two Surgical Approaches in the Treatment of Degenerative Spondylolysthesis
NCT00869882 ·Status: COMPLETED ·Phase: NA
-
Lumbar Fusion With The Icotec CF/PEEK Pedicle System In Combination With The Icotec CF/PEEK TLIF Cage ETurn™
NCT02087267 ·Status: COMPLETED
-
Efficacy and Safety of Novosis Putty for Degenerative Lumbar Disease
NCT06715345 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Gait and Postural Stability Assessment in Children With Idiopathic Scoliosis Undergoing Posterior Spine Instrumentation
NCT01109082 ·Status: COMPLETED
-
Midline Lumbar Fusion Versus Posterior Lumbar Interbody Fusion
NCT02290314 ·Status: UNKNOWN ·Phase: NA
-
Sagittal Plane Correction With Pass-LP Device in Adult Deformity Patients
NCT01635322 ·Status: COMPLETED
-
Instr. vs. Non-instr. Posterolateral Spinal Fusion in Patients With Spinal Stenosis and Degenerative Listhesis
NCT04166981 ·Status: COMPLETED ·Phase: NA
-
Clinical Evidence of Robot Guided vs. Navigated vs. Free Hand Lumbar Spinal Fusion
NCT02998060 ·Status: WITHDRAWN ·Phase: NA
-
A Study to Evaluate the Safety and Effectiveness of the TOPS™ SP System
NCT03247166 ·Status: UNKNOWN ·Phase: NA
-
Fibergraft Interbody Fusion Retrospective
NCT03898232 ·Status: COMPLETED
-
Interbody vs Instrumented Posterolateral Fusion Following Decompression for Lumbar Spinal Stenosis With Degenerative Spondylolisthesis
NCT01921530 ·Status: UNKNOWN ·Phase: PHASE4
-
Direct Repair Surgery for Spondylolysis of Lumbar in Young Population
NCT02129374 ·Status: COMPLETED ·Phase: NA
-
Isthmic Spondylolisthesis Treated With Combined Approach: Clinical and Radiological Outcomes
NCT03585439 ·Status: COMPLETED
-
NanOss Bioactive With Autograft and Bone Marrow Aspirate in the Posterolateral Spine
NCT02005341 ·Status: WITHDRAWN ·Phase: NA
-
Safety and Efficacy Study of NeoFuse in Subjects Requiring Posterolateral Lumbar Fusion
NCT00810212 ·Status: WITHDRAWN ·Phase: PHASE1/PHASE2
-
Safety and Preliminary Effectiveness of NVD-001 for the Treatment of Low Grade Degenerative Lumbar Spondylolisthesis
NCT03100032 ·Status: COMPLETED ·Phase: PHASE1/PHASE2