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Prospective Registry to Evaluate Outcomes of NanoBone® Bone Graft in Acute Trauma
Sponsor: Artoss Inc.
Summary
This multicenter prospective patient registry was developed with the aim of documenting how orthopedic surgeons are utilizing the NanoBone products in acute trauma cases along with relevant patient outcomes. These outcomes include radiographic measures such as fracture healing, instrumentation integrity, and clinical outcomes (symptom and function improvement) based on investigator and patient-based outcome assessments.
Official title: Multicenter Prospective Registry to Evaluate Use and Outcomes of NanoBone® Bone Graft Substitute in Acute Trauma Patients
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
OBSERVATIONAL
Enrollment
200
Start Date
2023-12-01
Completion Date
2026-12-01
Last Updated
2025-02-12
Healthy Volunteers
No
Conditions
Interventions
NanoBone® Bone Graft
The surgical technique used by the surgeon and the choice of the specific NanoBone product is or was determined solely by the surgeon and is independent of this observational study.
Locations (1)
SSM Health St. Mary's Hospital
Madison, Wisconsin, United States