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OssDsign® Spine Registry Study ("Propel")

Launched by OSSDSIGN · Apr 8, 2022

Trial Information

Current as of June 27, 2025

Recruiting

Keywords

Synthetic Bone Grafts Degenerative Disc Disease Bone Fusion

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.

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

0 patients applied

Trial Officials

Melanie Marshall

Study Director

OssDsign

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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