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Study identifier: NCT05329129 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

OssDsign® Spine Registry Study ("Propel")

Condition: Degenerative Disc Disease · Spinal Stenosis  ·  Sponsor: OssDsign

PhaseN/A
Planned participants450
Who can joinAll sexes, 21 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

jeff Feldhaus  ·  13476694903  ·  jfeldhaus@msquaredassociates.com

Pete weiman  ·  13479540542  ·  pete.weiman@propharmagroup.com

Always discuss trial participation with your own doctor first.

Locations (15)

Community Health Partners NeuroscienceFresno, California, United StatesRecruiting
Memorial Orthopaedic Surgical GroupLong Beach, California, United StatesRecruiting
San Diego NeurosurgerySan Diego, California, United StatesTerminated
Orthopedic Associates of HartfordHartford, Connecticut, United StatesActive Not Recruiting
Central Connecticut Neurosurgery and SpineNew Britian, Connecticut, United StatesRecruiting
Yale Center for Clinical Investigation, Yale School of MedicineNew Haven, Connecticut, United StatesRecruiting
Minimally Invasive Spine Center of South FloridaMiami, Florida, United StatesRecruiting
Foundation for Orthopaedic Research and EducationTampa, Florida, United StatesRecruiting
Northeast Georgia Medical CenterGainesville, Georgia, United StatesActive Not Recruiting
Carle Foundation Hospital, NeuroScience InstituteUrbana, Illinois, United StatesCompleted
Orthopaedic Institute of Western KentuckyPaducah, Kentucky, United StatesCompleted
OrthoBethesda Research FoundationBethesda, Maryland, United StatesActive Not Recruiting

+ 3 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT05329129