OssDsign® Spine Registry Study ("Propel")
Launched by OSSDSIGN · Apr 8, 2022
Trial Information
Current as of June 27, 2025
Recruiting
Keywords
ClinConnect Summary
The OssDsign® Spine Registry Study, also known as "Propel," is a clinical trial that aims to collect information about how well a specific type of bone graft substitute works for patients undergoing spine fusion surgery. This study focuses on patients with conditions like degenerative disc disease and spinal stenosis. The main goal is to understand the real-world effectiveness of OssDsign® bone grafts in helping patients heal after their surgery.
To participate in this study, patients need to be at least 21 years old and have been recommended for spinal fusion surgery where the OssDsign® bone graft is considered suitable by their surgeon. Participants should be able to follow the study's guidelines, which include attending follow-up appointments and completing necessary paperwork for up to two years after their surgery. This study is still enrolling participants, so it's a great opportunity for those who qualify to contribute to important research while receiving care for their spine condition.
Gender
ALL
Eligibility criteria
- • The patient has been diagnosed as a candidate for spinal fusion surgery for which the surgeon has decided an OssDsign® bone graft is appropriate.
- • The patient is ≥21 years old.
- • The patient is, in the investigator's opinion, psychosocially, mentally, and physically able to fully comply with this protocol, including the post-operative regimen, required follow-up visits, the filling out of required forms, and have the ability to understand and give written informed consent
- • The patient is willing and able to participate in post- operative clinical and radiographic follow up evaluations for 2 years.
- Exclusion Criteria:
- • Patients not meeting all of the inclusion criteria
About Ossdsign
Ossdsign is a pioneering clinical trial sponsor focused on advancing innovative solutions in the field of orthopedic and musculoskeletal health. With a commitment to enhancing patient outcomes, Ossdsign specializes in the development of cutting-edge diagnostic and therapeutic technologies that leverage advanced biomaterials and data-driven methodologies. The organization collaborates with leading healthcare professionals and research institutions to conduct rigorous clinical trials aimed at validating the efficacy and safety of its products. By fostering a culture of scientific excellence and patient-centric innovation, Ossdsign strives to contribute significantly to the future of orthopedic care and improve the quality of life for patients worldwide.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Gainesville, Georgia, United States
State College, Pennsylvania, United States
Edina, Minnesota, United States
Paducah, Kentucky, United States
Bethesda, Maryland, United States
Tampa, Florida, United States
Bethesda, Maryland, United States
Hartford, Connecticut, United States
San Diego, California, United States
Urbana, Illinois, United States
Miami, Florida, United States
New Haven, Connecticut, United States
Fresno, California, United States
New Britian, Connecticut, United States
Patients applied
Trial Officials
Melanie Marshall
Study Director
OssDsign
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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