Orthopaedic Institute of Western Kentucky

Paducah, Kentucky 42003

1 studies enrolling now · 21 studies all time

What they study most

Ankle Arthropathy, Cervical Degenerative Disc Disorder, Cervical Disc Disease, Degenerative Disc Disease, Herniated Disk, Herniated Lumbar Disk, Lumbar Degenerative Disc Disease, Lumbar Disc Herniation, Lumbar Spine Disc Herniation, Lumbar Spine Disease, Lumbar Spine Instability, Lumbar Spondylolisthesis

Studies at this site

• OssDsign® Spine Registry Study ("Propel") — Recruiting now
• Post Approval Study Protocol for the Two Level Simplify® Cervical Artificial Disc — Completed
• Investigation of the Two Level Simplify® Cervical Artificial Disc — Completed
• Post-Approval Study Protocol for the Simplify Cervical Artificial Disc — Completed
• Advanced Materials Science in XLIF Study — Enrolling by invitation
• P-15L Bone Graft in Transforaminal Lumbar Interbody Fusion With Instrumentation — Running, not enrolling
• 2-level Cervical Disc Replacement Comparing Prodisc C SK & Vivo to Mobi-C — Running, not enrolling
• Cervical Interbody Fusion Device Patient Registry — Stopped early
• Confirmatory Clinical Study of Oxiplex — Completed
• A Clinical Trial Comparing the BAGUERA C to the Marketed Mobi-C® for the Treatment of Single Level Cervical Disc Disease — Status unconfirmed
• Prospective, Multi-center Study to Assess Posterolateral Fusion Using FIBERGRAFT — Completed
• Clinical Evaluation of Fortilink® TETRAfuse® Interbody Fusion Device in Subjects With Degenerative Disc Disease — Completed
• A Clinical Trial Comparing the BAGUERA C to the Marketed Mobi-C® for the Treatment of Cervical Disc Disease at 2 Contiguous Levels — Running, not enrolling
• Retrospective Evaluation of Clinical and Radiographic Outcomes Following Total Talus Replacement — Completed
• Post Marketing Study of MagnetOs Putty Compared to Local Autograft in Patients Undergoing Posterolateral Lumbar Fusion — Completed
• Rampart Duo Clinical (RaDical) Post-Market Study — Completed
• Lumbar Discectomy Control Study, Risk Factors for Reherniation — Status unconfirmed
• Study of Lumbar Discectomy With Annular Closure — Status unconfirmed
• OSTEOAMP Lumbar Fusion Intra-Patient Controlled Study — Status unconfirmed
• Novum Vitrium® Cervical Cage in Anterior Cervical Discectomy and Fusion — Stopped early
• Burst Biologics Spinal Fusion Registry — Status unconfirmed