OssDsign® Spine Registry Study ("Propel") (NCT05329129)
PROSPECTIVE OBSERVATIONAL SPINE FUSION REGISTRY FOR OssDsign® BONE GRAFT SUBSTITUTES IN REAL WORLD CLINICAL PRACTICE
🩺 Plain-English Summary (8th-Grade Level)
The purpose of this multi-center, prospective, observational registry is to gather information on the clinical outcomes and real-world use of commercially available bone graft substitutes manufactured by OssDsign® AB, in patients who require spine fusion.
Who can join: Review the eligibility criteria below.
Location: Community Health Partners Neuroscience — Fresno, California
Age range: 21 Years
🧪 Interventions in This Study
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (15 Sites)
- Community Health Partners Neuroscience — Fresno, California
- Memorial Orthopaedic Surgical Group — Long Beach, California
- San Diego Neurosurgery — San Diego, California
- Orthopedic Associates of Hartford — Hartford, Connecticut
- Central Connecticut Neurosurgery and Spine — New Britian, Connecticut
- Yale Center for Clinical Investigation, Yale School of Medicine — New Haven, Connecticut
- Minimally Invasive Spine Center of South Florida — Miami, Florida
- Foundation for Orthopaedic Research and Education — Tampa, Florida
- Northeast Georgia Medical Center — Gainesville, Georgia
- Carle Foundation Hospital, NeuroScience Institute — Urbana, Illinois
- Orthopaedic Institute of Western Kentucky — Paducah, Kentucky
- OrthoBethesda Research Foundation — Bethesda, Maryland
- Twin Cities Orthopedics — Edina, Minnesota
- University Orthopedics Center — State College, Pennsylvania
- Texas Spine Consultants — Addison, Texas
📞 Contact the Study Coordinator
Phone: (347) 669-4903
Email: jfeldhaus@msquaredassociates.com
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
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💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.