Comparison of Iliac Crest Marrow vs. Proximal Tibia Avitus® Bone Graft
ConditionBone Graft
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-70
SponsorMayo Clinic
About this trial
The purpose of this research is to provide comparative data about the Avitus product and its equivalence to other Bone Marrow Aspirate (BMA) harvesting techniques.
Eligibility criteria
Qualifiers
Patient must be 18 years of age or older.
Patient must be able and willing to sign the IRB approved informed consent.
Patient must consent to preoperative knee and pelvis radiographs to confirm no issue at harvest location.
Patient has indication for autograft bone harvest (undergoing any ankle or hindfoot fusion, complex mid and forefoot fusions requiring graft supplementation, treatment of fuse and fracture nonunions)
Disqualifiers
Patient is 70 yrs of age or older.
Patient is unwilling or unable to give consent or comply with study protocol.
Patient has any condition, which in the judgement of the Investigator, places the patient at undue risk or interferes with the study.
Patient has mental or neurological disorder that will not allow for proper informed consent.
Trial design
Treatments tested in this trial
- Avitus Bone Harvester
Treatment groups
12 Participants
are divided into 1 treatment groupSponsors and collaborators
Mayo Clinic
Lead sponsor
Zimmer Biomet
Collaborator
Source ClinicalTrials.gov