Prospective Study on Safety and Performance of Surgalign spINE Products
Status: Recruiting
Location: See all (12) locations...
Intervention Type: Device
Study Type: Observational
SUMMARY
This study is a prospective, multi-center, open label registry designed to collect real-world data on performance and safety data on RTI's spine products.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:
• Candidate for RTI spine product.
• Willing and able to consent to the study.
Locations
United States
Connecticut
Hartford Hospital
ACTIVE_NOT_RECRUITING
Hartford
Florida
Florida Back Institute
ACTIVE_NOT_RECRUITING
Boca Raton
Spine Institute of South Florida
ACTIVE_NOT_RECRUITING
Delray Beach
Illinois
Suburban Orthopaedics
TERMINATED
Bartlett
Indiana
Indiana Spine Group
WITHDRAWN
Carmel
DK Orthopedics
COMPLETED
Crown Point
Ohio
Lindner Center for Research & Education at The Christ Hospit
ACTIVE_NOT_RECRUITING
Cincinnati
Other Locations
Germany
STENUM Ortho Fachklinik
WITHDRAWN
Ganderkesee
Wirbelsäulenzentrum Fulda | Main | Kinzig
ACTIVE_NOT_RECRUITING
Gelnhausen
Katholisches Klinikum Koblenz - Montabaur
WITHDRAWN
Koblenz
St. Christopherus Krankenhaus - Katholisches Klinikum
WITHDRAWN
Werne
Spain
Hospital Nacional de Parapléjicos
RECRUITING
Toledo
Contact Information
Primary
Isabella M Rosales, BS
irosales@xtantmedical.com
406-924-5884
Backup
Laura Henderson
lhenderson@xtantmedical.com
406-813-4107
Time Frame
Start Date: 2020-01-28
Estimated Completion Date: 2025-06
Participants
Target number of participants: 5000
Related Therapeutic Areas
Sponsors
Leads: Xtant Medical