A Clinical Trial Comparing the BAGUERA C to the Marketed Mobi-C® for the Treatment of Cervical Disc Disease at 2 Contiguous Levels
- Conditions
- Cervical Disc Disease
- Interventions
- Device: BAGUERA®C Cervical Disc ProsthesisDevice: Mobi-C Cervical Disc
- Registration Number
- NCT04564885
- Lead Sponsor
- Spineart USA
- Brief Summary
The proposed investigation is a multi-center, prospective, randomized, controlled comparison of the BAGUERA®C to the control, a similar, legally marketed total disc replacement device in subjects with symptomatic cervical disc disease (SCDD) at two contiguous levels. Subjects will be randomized in a 2:1 ratio to the two-level BAGUERA®C Cervical Disc Prosthesis (investigational group) or to the two-level Mobi-C® Cervical Disc (control group). Subjects enrolled in the study will be evaluated pre-operatively, at the time of surgery, discharge, and at 6 weeks, 3, 6, 12, and 24 months and then annually until 7 years post-surgery.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- All
- Target Recruitment
- 300
Not provided
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description BAGUERA®C BAGUERA®C Cervical Disc Prosthesis surgical placement of the BAGUERA®C Cervical Disc Prosthesis at 2 contiguous levels Mobi-C® Mobi-C Cervical Disc surgical placement of the Mobi-C® Cervical Disc at 2 contiguous levels
- Primary Outcome Measures
Name Time Method Procedure or device related serious adverse events 24 month follow-up visit No serious adverse event(s) confirmed as device or procedure related as adjudicated by the Clinical Events Committee
Neck Disability Index 24 month follow-up visit at least a 15 percentage point improvement (decrease) from baseline on a 0 - 100% scale
No secondary surgical intervention per protocol definition 24 month follow-up visit any revision, removal, re-operation, or supplemental fixation at the index level
Maintenance or improvement in neurological status 24 month follow-up visit pre and post-op neurological examination to determine maintenance or improvement
- Secondary Outcome Measures
Name Time Method
Related Research Topics
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Trial Locations
- Locations (26)
BEEL Medical
🇺🇸Laguna Hills, California, United States
Eisenhower Medical Center
🇺🇸Rancho Mirage, California, United States
Orthopaedic Institute of Western Kentucky
🇺🇸Paducah, Kentucky, United States
Legacy Brain & Spine
🇺🇸Atlanta, Georgia, United States
Midwest Orthopedics at Rush
🇺🇸Chicago, Illinois, United States
NorthShore
🇺🇸Evanston, Illinois, United States
The Ohio State University - Dept of Orthadedics
🇺🇸Columbus, Ohio, United States
Indiana Spine Group
🇺🇸Carmel, Indiana, United States
Ortho NorthEast
🇺🇸Fort Wayne, Indiana, United States
Spine Institute of Louisiana Foundation
🇺🇸Shreveport, Louisiana, United States
Center for Sports Medicine & Orthopedics
🇺🇸Chattanooga, Tennessee, United States
The Spine Institute, Center for Spine Restoration
🇺🇸Santa Monica, California, United States
UCI Health
🇺🇸Orange, California, United States
Institute for Neuro Innovation
🇺🇸West Hills, California, United States
The Disc Replacement Center
🇺🇸Salt Lake City, Utah, United States
MORE Foundation
🇺🇸Phoenix, Arizona, United States
Desert Institute for Spine Care
🇺🇸Scottsdale, Arizona, United States
Orange County Neurosurgical Associates
🇺🇸Mission Viejo, California, United States
Hartford Health CT Orthopaedics
🇺🇸Hamden, Connecticut, United States
Vail-Summit Orthopaedics and Neurosurgery
🇺🇸Vail, Colorado, United States
Georgetown University Medical Center
🇺🇸Washington, District of Columbia, United States
Carolina Neurosurgery and Spine Associates
🇺🇸Charlotte, North Carolina, United States
Neurosurgical Associates of Lancaster
🇺🇸Lancaster, Pennsylvania, United States
Oregon Spine Care
🇺🇸Tualatin, Oregon, United States
St. David's Healthcare
🇺🇸Austin, Texas, United States
Swedish Neuroscience, Swedish Spine Institute
🇺🇸Seattle, Washington, United States