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A Prospective, Multi-Center, Nonrandomized Study to Assess Lumbar Fusion Using Interbody Cages With Autograft in Conjunction With Instrumented Posterolateral Gutter Fusions Using NanOss Bioactive
Conditions
Interventions
nanOss Bioactive Bone void filler
Interbody FCage
Locations
7
United States
Tower Orthopaedics & Neurosurgical Spine Institute
Beverly Hills, California, United States
Scripps Memorial Hospital Neurosurgery
La Jolla, California, United States
Northwestern Medical Facility
Chicago, Illinois, United States
Advanced Center for Orthopedics
Marquette, Michigan, United States
St. Johns Spine and Pain Clinic
Springfield, Missouri, United States
Medical University of South Carolina Neurology
Charleston, South Carolina, United States
Start Date
July 1, 2010
Primary Completion Date
September 1, 2013
Completion Date
September 1, 2013
Last Updated
December 7, 2016
NCT04992572
NCT07254806
NCT06886802
NCT05508360
NCT05037968
NCT05029726
Lead Sponsor
Pioneer Surgical Technology, Inc.
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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