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Prospective Registry to Evaluate Outcomes of NanoBone® Bone Graft in Acute Trauma

Multicenter Prospective Registry to Evaluate Use and Outcomes of NanoBone® Bone Graft Substitute in Acute Trauma Patients

Who can join

Ages 18 and older · All sexes

Inclusion Criteria:

1. Subjects at least 18 years old at the time of injury
2. Acute fractures, resulting from blunt or penetrating trauma

   * In the extremities or pelvis
   * Requiring surgery
   * Treated emergently, delayed or staged up to 4 weeks from the date of injury
   * Where bone grafting is clinically indicated

Exclusion Criteria:

1. Certain fracture locations (these apply to non-unions as well)

   * Hand - metacarpals, phalanges
   * Forefoot - metatarsals, phalanges
   * Skull
   * Spine
2. Fractures requiring definitive fracture stabilization beyond the initial 4 weeks from the date of injury
3. Pathologic fractures secondary to malignancy
4. Subjects unable to follow recommended post-operative plan and complete follow ups
5. Subjects unable to complete patient reported outcome measures

About the study

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.

What is being tested

• NanoBone® Bone Graft (device)

Sponsor: Artoss Inc. · Participants: 200 · Started: Dec 1, 2023

Contact the study team

• James J Cassidy, Ph.D. · Phone: 320-259-4321

Official record on ClinicalTrials.gov — NCT06256458

Locations in the U.S.

Conditions

• Fractures

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.