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Spinal Fusion

Clinical trial condition

Spinal Fusion

Explore clinical trials studying Spinal Fusion. Study availability and eligibility vary by location and protocol.

74 public trials 18 recruiting studies

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Spinal Fusion trial results

Completed

Use of Activated Recombinant FVII in Spinal Surgery

NCT00102037

Conditions: Acquired Bleeding Disorder, Spinal Fusion
Locations: Novo Nordisk Investigational Site Sacramento, California, United States

Novo Nordisk Investigational Site San Francisco, California, United States

Novo Nordisk Investigational Site Washington D.C., District of Columbia, United States

Novo Nordisk Investigational Site Miami, Florida, United States

View all 14 locations

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Completed

Point of Care Testing in Pediatric Patients Undergoing Major Surgery

NCT01742936

Conditions: Cardiopulmonary Bypass, Spinal Fusion
Locations: Nationwide Children's Hospital Columbus, Ohio, United States

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Completed

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

NCT01136590

Conditions: Antifibrinolytic Agents, Blood Transfusion, Hemorrhage, +3 more
Locations: Hospital Clinic de Barcelona Barcelona, Spain

Hospital Vall d'Hebron de Barcelona Barcelona, Spain

Hospital de Bellvitge L'Hospitalet de Llobregat, Barcelona, Spain

Hospital de Getafe Getafe, Madrid, Spain

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Completed

Remifentanil Propofol Infusion in Pediatric Spinal Surgery

NCT00761072

Conditions: Spinal Fusion
Locations: The Children's Hospital of Philadelphia Philadelphia, Pennsylvania, United States

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Completed

Prevalence of Inadvertent Hyperventilation During Intraoperative Anesthetic Care

NCT01235650

Conditions: Spinal Fusion
Locations: Not specified

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Completed

Is Pleth Variability Index (PVI) a Surrogate for Pulse Pressure Variations (PPV) in Pediatric Spine Fusion (SF) Surgery?

NCT00994656

Conditions: Bone Diseases, Hypovolemia, Musculoskeletal Diseases, +6 more
Locations: The Children's Hospital of Philadelphia Philadelphia, Pennsylvania, United States

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Completed

Bioactive Glass as Bone Graft Substitute in Operative Treatment of Bone - a 10 Years Follow-up Study

NCT00935870

Conditions: Benign Bone Tumour Cavity, Depressed Lateral Condyle Fracture, Spinal Fusion
Locations: Turku University Hospital Turku, Finland

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Completed

Use of Radiostereometric Analysis (RSA) Following Spinal Fusion Versus the DYNESYS Stabilization System

NCT00152165

Conditions: Orthopedic Procedures, Spinal Fusion
Locations: Institute for Human Performance Syracuse, New York, United States

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Completed

Use of Radiostereometric Analysis Beads (RSA) to Measure Motion in the Spine, Following Lumbar Spinal Surgery

NCT00152152

Conditions: Lumbar Discectomy, Spinal Fusion
Locations: SUNY Upstate Medical University Syracuse, New York, United States

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Active, Not Recruiting

Lumbar Fusion With Porous Versus Non-Porous Cages

NCT05583864

Conditions: Ankylosis, Arthrodesis, Bone Diseases, +12 more
Locations: University of Kentucky Lexington, Kentucky, United States

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