CopiOs(TM) Bone Void Filler in the Post-Harvest Iliac Crest
NCT00768924 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 35
Last updated 2011-09-30
Summary
The CopiOs Bone Void Filler (BVF) is a synthetic bone graft material consisting of calcium phosphate dehydrate within lyophilized type I bovine collagen that has been formed into pads of various sizes for surgical implantation. Pre-clinical animal studies suggest that the bone healing strength of CopiOs to be equivalent to autograft.
Conditions
- Spinal Fusions
Sponsors & Collaborators
-
Zimmer Biomet
lead INDUSTRY
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2007-03-31
- Primary Completion
- 2007-12-31
- Completion
- 2008-12-31
Countries
- United States
Study Locations
More Related Trials
-
Comparison of a Bone Product to Bone Dust in Ossification of Small Calvarial Defects.
NCT01006148 ·Status: WITHDRAWN ·Phase: PHASE4
-
A Clinical Study of the Use of Brushite as Primary Stabilizer in Immediate Dental Implantation
NCT00299585 ·Status: SUSPENDED ·Phase: PHASE2
-
Vitoss With Bone Marrow Aspirate Versus Prodense
NCT03509480 ·Status: COMPLETED ·Phase: NA
-
Assessment of Bone Gain Following Composite Graft Rehabilitation of Horizontal Maxilla Atrophy With Sausage Technique Utilizing (Pericardial) Collagen Membrane
NCT06831214 ·Status: RECRUITING ·Phase: NA
-
Use of Particulate Cortico- Cancellous Anterior Iliac Graft with Periosteum Membrane in Unilateral Alveolar Cleft Grafting Versus Particulate Cortico-cancellous Anterior Iliac Grafting Alone.
NCT06795919 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Bone Remodeling After Immediate Implant Placement With and Without Bone Grafting
NCT02174198 ·Status: COMPLETED ·Phase: NA
-
Lateral Ridge Augmentation Using a Volume Maintaining Collagen Scaffold Versus Allograft With Collagen Membrane.
NCT03457298 ·Status: UNKNOWN ·Phase: NA
-
The Use of RIA to Harvest Bone Graft for Treatment of Non-unions and Fractures
NCT00582439 ·Status: COMPLETED ·Phase: NA
-
Deproteinized Bovine Bone in Alveolar Bone Critical Size Defect (>2cm) Secondary to Cyst Removal
NCT02612740 ·Status: COMPLETED ·Phase: PHASE2
-
Alveolar Cleft Grafting by Double Iliac Bone Blocks Versus Iliac Spongy Bone From Anterior Iliac Crest
NCT05283005 ·Status: UNKNOWN ·Phase: NA
-
Evaluating the Impact of Prefabricated Acrylic Splints on Premaxillary Stability in Alveolar Cleft Bone Graft Repairs: a Randomized Controlled Trial
NCT06807645 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Synthetic Cranioplasty PEEK Versus UHMWP
NCT05250024 ·Status: COMPLETED ·Phase: NA
-
In Vivo Clinical Trial of Porous Starch - Hydroxyapatite Composite Biomaterials for Bone Regeneration
NCT02910232 ·Status: COMPLETED
-
Filling Bone Defects/Voids With Autologous BonoFill-II for Maxillofacial Bone Regeneration
NCT02842619 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
BonyPid-500TM Bone Graft Substitute Study
NCT02531100 ·Status: COMPLETED ·Phase: NA
-
Calcium Phosphate Cement As Bone Void Filler
NCT04645186 ·Status: TERMINATED
-
Using Boned-Apatite Cement at the Time of Extraction for Ridge Preservation at These Sites
NCT02440048 ·Status: COMPLETED ·Phase: NA
-
Osteoconduction Potential of an Injectable Calcium Phosphate in Orthopaedic Surgery in Fillings of Osseous Defects
NCT00206791 ·Status: COMPLETED ·Phase: NA
-
Circumferential Vertebral Reconstruction of Osteoporotic Compression Fractures Using a Novel Bipedicular Peek Implant
NCT05337696 ·Status: TERMINATED ·Phase: NA
-
Complete Twelve Month Bone Remodeling With a Bi-phasic Injectable Bone Substitute in Benign Bone Tumors
NCT02567084 ·Status: COMPLETED ·Phase: NA
-
Ridge Preservation Using a Ossix™ Bone vs Bio-Oss® Collagen
NCT04338516 ·Status: COMPLETED ·Phase: NA
-
Bone Substitutes Outcomes - Post Market Follow-up
NCT06374342 ·Status: RECRUITING
-
SINUS LIFT 100% Anorganic Bovine Bone vs. 50% Anorganic Bovine Bone + 50% Autologous Bone
NCT02170129 ·Status: COMPLETED ·Phase: NA
-
Evaluation of a Synthetic Bone Substitute for Ridge Preservation
NCT02894528 ·Status: COMPLETED ·Phase: PHASE4
-
Study to Evaluate the Effectivity and Safety of BIOSCAFF®H Compared to DuraGen®, in Patients Undergoing Dural Repair
NCT06419855 ·Status: TERMINATED