ViBone in Cervical and Lumbar Spine Fusion
NCT03425682 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 118
Last updated 2025-03-04
Summary
Assess clinical and radiographic outcomes in patients who undergo 1-3 level anterior cervical discectomy fusion (ACDF) or lumbar interbody fusion (TLIF, PLIF, ALIF, or LLIF) using ViBone.
Conditions
- Spondylosis
- Cervical Spondylosis
- Spondylolisthesis
- Herniated Nucleus Pulposus
- Degenerative Disc Disease
Interventions
- OTHER
-
ViBone
Viable Bone Allograft
Sponsors & Collaborators
-
Elutia Inc.
lead INDUSTRY
Eligibility
- Min Age
- 18 Years
- Max Age
- 80 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2018-05-14
- Primary Completion
- 2021-01-15
- Completion
- 2021-06-30
Countries
- United States
Study Locations
More Related Trials
-
Prospective Comparative Analysis of ACDF vs Fusion Interbody Cages With nanoLOCK Osseointegrative Technology
NCT05762055 ·Status: ENROLLING_BY_INVITATION ·Phase: NA
-
Accell Evo3™ Demineralized Bone Matrix in Instrumented Lumbar Spine Fusion
NCT02018445 ·Status: COMPLETED ·Phase: NA
-
A Pre-market Study to Evaluate b.Bone for Posterolateral Fusion (b.Spine Clinical Trial).
NCT05906394 ·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
-
Efficacy and Safety of Accell Evo3 Demineralized Bone Matrix (DBM) in Instrumented Posterolateral Lumbar Spine Fusion
NCT01430299 ·Status: COMPLETED ·Phase: NA
-
Safety Study of Preservon-Treated Bone Implants for Cervical Fusion in the Treatment of Cervical Radiculopathy or Myelopathy
NCT00344890 ·Status: COMPLETED ·Phase: NA
-
Posterior Cervical Fixation Study
NCT04770571 ·Status: ENROLLING_BY_INVITATION
-
A Prospective Study of NuCel® in Cervical Spine Fusion
NCT02381067 ·Status: TERMINATED ·Phase: NA
-
Patient Registry to Observe Outcomes Following Implantation of the VariLift Interbody Fusion Device
NCT01944345 ·Status: COMPLETED
-
Adjacent Level Anterior Cervical Fusion: SeaSpine Shoreline Versus Removal of Previously Implanted Plate and Replating
NCT06415136 ·Status: ENROLLING_BY_INVITATION
-
PMCF Study to Evaluate the VERTICALE® Cervical System in Spine Surgery According to Its Intended Use.
NCT05489822 ·Status: TERMINATED
-
Allogeinic Bone Paste
NCT04605120 ·Status: UNKNOWN ·Phase: NA
-
Efficacy and Safety of Integra Accell Evo3 DBM in Instrumented Lumbar Spine Fusion
NCT01714804 ·Status: COMPLETED ·Phase: NA
-
Cellentra Viable Cell Bone Matrix (VCBM) Anterior Cervical Discectomy and Fusion Outcomes Study (VCBM/MaxAn)
NCT02182843 ·Status: COMPLETED ·Phase: NA
-
A Retrospective Study of Actifuse Synthetic Bone Graft Versus Other Bone Graft Substitutes in Patients Requiring Lumbar Fusion
NCT01833962 ·Status: UNKNOWN
-
M6-C Artificial Cervical Disc Two-Level IDE Pivotal Study
NCT04982835 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Osteocel® Plus in Anterior Cervical Discectomy and Fusion (ACDF)
NCT00942045 ·Status: COMPLETED
-
Lumbar & Sacroiliac Fusion Study Involving Previously Implanted Devices
NCT07204288 ·Status: RECRUITING ·Phase: NA
-
Evaluation of Outcomes for Quality of Life and Activities of Daily Living for BKP in the Treatment of VCFs
NCT01871519 ·Status: COMPLETED ·Phase: NA
-
Prospective, Multicenter, Case-Control Analysis of the VersaTie Posterior Fixation System to Prevent Proximal Junctional Failure in Long Posterior Spinal Fusion Constructs for Adult Patients
NCT04888104 ·Status: RECRUITING
-
Natural Matrix Protein™ (NMP™) Fibers in Cervical and Lumbar Interbody Fusion
NCT06000319 ·Status: ENROLLING_BY_INVITATION
-
An Assessment of P-15 Bone Putty in Anterior Cervical Fusion With Instrumentation
NCT00310440 ·Status: COMPLETED ·Phase: NA
-
OsteoStrux™ Collagen Ceramic Scaffold in Instrumented Lumbar Spine Fusion
NCT01873586 ·Status: COMPLETED ·Phase: NA
-
Artoss Prospective Spine Registry Outcomes
NCT04439032 ·Status: ACTIVE_NOT_RECRUITING
-
Treatment of One and/or Two Level Cervical Degenerative Disc Disease
NCT05812092 ·Status: ENROLLING_BY_INVITATION