Status | Study |
Withdrawn |
Study Name: The PRIORi-T Trial--Prospective Randomized Investigation of Radiofrequency Targeted Vertebral Augmentation Condition: Painful Osteoporotic Vertebral Compression Fractures (VCF) Date: 2011-11-23 Interventions: Device: Vertebral Augmentation (STABILIT) |
Withdrawn |
Study Name: Evaluation of Vertebral Compression Fracture Fixation With RF Kyphoplasty in Patients With Multiple Myeloma Condition: Multiple Myeloma Compression Fracture of Vertebral Column Date: 2011-08-04 Interventions: Procedure: Kyphoplasty/Vertebral Augmentation (Device-StabiliT) Targeted Vertebral Augmentation for the |
Withdrawn |
Study Name: Evaluating Vertebroplasty and Kyphoplasty for Reducing Trauma-related Fractures Condition: Vertebral Body Compression Fractures Date: 2011-07-25 Interventions: Procedure: Kyphoplasty Patient |
Completed |
Study Name: Unipedicular vs. Bipedicular Kyphoplasty for the Treatment of Osteoporotic Vertebral Fractures Condition: Vertebral Compression Fracture Date: 2011-06-13 Interventions: Device: Kyphon® Balloon Kyphoplasty (Kyphon Inc; Sunnydale, CA) A Jamshidi Crown Bone Biopsy Needle |
Completed |
Study Name: The Prevalence of Osteoporotic Vertebral Compression Fractures (OVCF) in Korean Post Menopausal Women Condition: Osteoporosis, Postmenopausal Date: 2011-06-09 Interventions: Other: Fracture evaluation DEXA(Dual-energy X-ray absorptiometry), X-ray |
Terminated |
Study Name: Dual-energy CT in Detecting Bone Marrow Edema of Vertebral Compression Fractures Condition: Compression Fracture of Thoracic Vertebral Body Spinal Date: 2011-01-20 |
Withdrawn |
Study Name: Vertebral Augmentation With Kyphoplasty vs Nonsurgical Mgmt for Vertebral Body Compression Fractures Condition: Multiple Myeloma Date: 2010-08-03 Interventions: Procedure: Vertebral Augmentation with Balloon Kyphoplasty |
Terminated |
Study Name: OsseoFix™ Spinal Fracture Reduction System in Treating Spinal Compression Fracture Condition: Vertebral Compression Fractures Date: 2009-08-17 Interventions: Device: OsseoFix Spinal Fracture Reduction System All enrolled into the study will be receiving the Osse |
Terminated |
Study Name: Anderson Circulating Tumor Cell Burden (CTCB) Study Condition: Cancer Spinal Disease Vertebral Comp Date: 2009-01-07 Interventions: Procedure: Kyphoplasty A small |
Completed |
Study Name: Medtronic SCORE Study - Study of Curette Use for Obtaining Restoration of Vertebral Body Anatomy in Balloon Kyphoplasty Condition: Vertebral Body Compression Fractures (VCFs) Date: 2008-12-12 Interventions: Device: Kyphon® Curette The Kyphon® Curette is intended to scrape and score bone in the spine. |