Research Trials Participated

  • Co-Investigator, *Clinical Trial*: Safety and Efficacy of Pulsed Electromagnetic Fields (Cervical-Stim) as an Adjunct to Enhance Union in Conservatively Treated, Orthofix, Inc.
  • Principal Investigator, *Clinical Trial*: Isolated Traumatic C1 Injury Patterns, Department of Neurological Surgery
    Grant #Invivo-100-101, Co-Investigator, *Clinical Trial*: INVIVO: Pilot Study of Clinical Safety and Feasibility of The Plga-Poly-L-Lysine Scaffold for The Treatment of Complete (ASIA A) Traumatic Acute Spinal Cord Injury, InVivo Therapeutics Corporation
  • Principal Investigator, *Clinical Trial*: A Prospective, Randomized, Multi-Center, Open-Label Pilot Study of Infuse® Bone Graft with Mastergraft® Strip and Posterior Fixation for Posterolateral Fusion (PLF) Treatment of Multi- Level Degenerative Lumbosacral Spinal Conditions, Medtronic, Inc
  • Co-Investigator, *Clinical Trial*: A Multicenter, Randomized, Double-Blind, Controlled Study of EXPAREL for Postsurgical Pain Management in Subjects Undergoing Open Lumbar Spinal Fusion Surgery, Pacira Pharmaceuticals, Inc.
  • Principal Investigator, Cost-effectiveness of a novel cervical spine clearance protocol: obviating the need for routine magnetic resonance imaging
  • Grant #MSB_DR003, Co-Investigator, *Clinical Trial*: A Prospective, Multi-center, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety, Mesoblast, Inc
  • Grant #VX15-210-101, Co-Investigator, *Clinical Trial*: A Phase 2b/3, Double-blind, Randomized, Placebo-Controlled, Mul5center Study to Assess the Efficacy and Safety of VX-210 in Subjects with Acute Trauma5c Cervical Spinal Cord Injury, Vertex Pharmaceuticals, Inc
  • *Clinical Trial*: Post-Market, 10 Year Follow Up of Mobi-C Cervical Disc for one and Two Level Treatment of Cervical Disc Disease, LDR Spine
  • Principal Investigator, *Clinical Trial*: Comparing clinical and radiographic outcomes of lumbar fixation techniques, Department of Neurological Surgery
  • Principal Investigator, *Clinical Trial*: Comparing clinical and radiographic outcomes of intramural tumors after surgical management, Department of Neurological Surgery
  • Principal Investigator, *Clinical Trial*: Tarlov’s cysts and clinical outcome after surgical and non-surgical intervention, Department of Neurological Surgery
  • Principal Investigator, *Clinical Trial*: Evaluation of Intraoperative Navigation and PediGuard for Pedicle Screw Insertion, Spine Guard, Inc.
  • Principal Investigator, *Clinical Trial*: 2-Level ACDF: A single Institution experience with multiple cervical devices, Department of Neurological Surgery
  • Grant #MSB_DR001 Disc, Co-Investigator, *Clinical Trial*: A Prospective, Multi-center, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety, Mesoblast, Inc
  • Grant #LDR-001, Co-Investigator, MOBI-C: A Multi-Center, Prospective, Randomized, Controlled Clinical Trial Comparing the Safety and Effectiveness of the MOBI-C Prosthesis to Conventional Anterior Cervical Discectomy and Fusion in the Treatment of Symptomatic Degenerative Disc Disease, LDR Spine
  • Co-Investigator, *Clinical Trial*: DuraSeal Exact Spine Sealant System Post-Approval Study, Integra
    Principal Investigator, *Clinical Trial*: Segmental Correction of Kyphotic Deformity, Department of Neurological Surgery
  • Principal Investigator, *Clinical Trial*: Does the Type of Procedure Affect the Incidence of Dysphagia and Dysphonia in ACDF patients?, Globus, Inc.