OssDsign® Spine Registry Study ("Propel")

Recruiting now

Conditions studied: Degenerative Disc Disease, Spinal Stenosis

In brief

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.

Key facts

Study ID

NCT05329129

Run by

OssDsign

People needed

450

Starts

2022-03-23

Expected to finish

2030-04-01

Last updated by the study team

2026-06-08

Who can join

Age: 21 and older. Sex: any. Healthy volunteers: not accepted.

You may not qualify if…

• Patients not meeting all of the inclusion criteria

Where it is running

• Community Health Partners Neuroscience — Fresno, California, United States (enrolling)
• Memorial Orthopaedic Surgical Group — Long Beach, California, United States (enrolling)
• Central Connecticut Neurosurgery and Spine — New Britian, Connecticut, United States (enrolling)
• Yale Center for Clinical Investigation, Yale School of Medicine — New Haven, Connecticut, United States (enrolling)
• Minimally Invasive Spine Center of South Florida — Miami, Florida, United States (enrolling)
• Foundation for Orthopaedic Research and Education — Tampa, Florida, United States (enrolling)
• University Orthopedics Center — State College, Pennsylvania, United States (enrolling)
• Texas Spine Consultants — Addison, Texas, United States
• Northeast Georgia Medical Center — Gainesville, Georgia, United States
• Carle Foundation Hospital, NeuroScience Institute — Urbana, Illinois, United States
• San Diego Neurosurgery — San Diego, California, United States
• Orthopedic Associates of Hartford — Hartford, Connecticut, United States
• Orthopaedic Institute of Western Kentucky — Paducah, Kentucky, United States
• OrthoBethesda Research Foundation — Bethesda, Maryland, United States
• Twin Cities Orthopedics — Edina, Minnesota, United States

Full record on ClinicalTrials.gov

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