Clinical Trials Logo
  1. Home
  2. Spinal Fusion
  3. NCT04439032

Artoss Prospective Spine Registry Outcomes — ASTRO  

Spinal Fusion Clinical Trial

Official title:
Multicenter Prospective Registry to Evaluate Use and Outcomes of NanoBone® Bone Graft Substitute in Spinal Fusion Surgery

Clinical Trial Summary

This prospective registry was designed as an observational study to ascertain how commercially available NanoBone Bone Graft is being used by surgeons performing spinal fusion as well as determining relevant patient outcomes.

Clinical Trial Description

This multicenter prospective patient registry was developed with the aim of documenting how spine and neurosurgeons are utilizing the NanoBone products along with relevant patient outcomes. These outcomes include radiographic measures such as fusion outcome, instrumentation integrity, and clinical outcomes (symptom and function improvement) based on investigator and patient-based outcome assessments. The primary objective of this study is to document and analyze the use of NanoBone products in spine fusion surgery (as a stand-alone bone graft, or in combination with local bone only, no other BGS or biologic product used) and determine both radiographic success and clinical outcomes. All product related adverse events will be documented, tabulated, and summarized. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04439032
Study type Observational
Source Artoss Inc.
Contact
Status Active, not recruiting
Phase
Start date August 3, 2020
Completion date December 2024
View Details
See also
  Status Clinical Trial Phase
Completed NCT04037059 - Impact of Body Habitus (Arm Span and Abdominal Girth) on Activities of Daily Living (ADL)
Recruiting NCT03883022 - Vancomycin Powder Combined With Autogenous Bone Graft as a Prevention for Post-operative Infection for Spine Surgery N/A
Not yet recruiting NCT06003010 - Yoga for Adolescent Idiopathic Scoliosis (AIS) Patients N/A
Completed NCT01235650 - Prevalence of Inadvertent Hyperventilation During Intraoperative Anesthetic Care N/A
Completed NCT01136590 - Multicenter, Randomized Placebo-controlled Clinical Trial to Evaluate the Effect of Perioperative Use of Tranexamic Acid on Transfusion Requirements and Surgical Bleeding in Major Spine Surgery Phase 4
Completed NCT03459404 - Sufentanil NanoTab PCA System/15 mcg for Acute Post-Operative Pain in Vertebral Surgery: A Preliminary Investigation
Recruiting NCT05010148 - A Clinical Trial of Intravenous Lidocaine After Spinal Surgery to Prevent Delirium and Reduce Pain Phase 3
Recruiting NCT04605120 - Allogeinic Bone Paste N/A
Completed NCT03826329 - Risk Factors of Second Surgery for Adjacent Segment Disease Following Anterior Cervical Discectomy and Fusion
Recruiting NCT04601363 - Personalized Spine Study Group (PSSG) Registry
Recruiting NCT05323448 - Efficacy of ARISTA-AH for Restoring Hemostasis Following Posterior Long-segment Spinal Fusion. N/A
Completed NCT00994656 - Is Pleth Variability Index (PVI) a Surrogate for Pulse Pressure Variations (PPV) in Pediatric Spine Fusion (SF) Surgery? N/A
Completed NCT00152152 - Use of Radiostereometric Analysis Beads (RSA) to Measure Motion in the Spine, Following Lumbar Spinal Surgery N/A
Terminated NCT03425799 - Efficacy and Safety of Tranexamic Acid in Spinal Fusion Surgery Phase 3
Not yet recruiting NCT06368245 - Durability of Suppl. Rod Constructs-SuppleMentAry Rod Technique for Long-segment Posterior Instrumented Spinal Fusions
Withdrawn NCT03908203 - Minimally Invasive Surgery Techniques for One-level Degenerative Lumbar Deformities Correction N/A
Terminated NCT03378973 - The Effects of Dexmedetomidine Dose on Motor Evoked Potentials Phase 4
Completed NCT05936047 - Bone Marrow Clot for Posterior Lumbar Fusion N/A
Not yet recruiting NCT03692845 - Minimally Invasive Versus Open Transforaminal Lumbar Interbody Fusion N/A
Completed NCT00152165 - Use of Radiostereometric Analysis (RSA) Following Spinal Fusion Versus the DYNESYS Stabilization System N/A