RecruitingNot ApplicableNCT07434505
Comparison of Iliac Crest Marrow vs. Proximal Tibia Avitus® Bone Graft
Sponsor
Mayo Clinic
Enrollment
12 participants
Start Date
Nov 6, 2025
Study Type
INTERVENTIONAL
Conditions
Summary
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
Min Age: 18 YearsMax Age: 70 Years
Inclusion Criteria8
- 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)
- Patient is indicated for proximal tibia autograft harvest and iliac crest BMA (e.g. no hx bilateral TKAs or previous iliac wing trauma bilaterally).
- Patient is skeletally "mature" and presents with no concern for osteopenia/osteoporosis.
- Patient has sufficient volume of harvest material for study inclusion (minimum of 10 ml of cancellous bone graft plus 10 ml fluid pressed out from cancellous bone portion)
- Patient must speak English or have access to sufficient translator.
Exclusion Criteria17
- 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.
- Patient is known to be pregnant or breastfeeding.
- Patient is a vulnerable subject (prisoner, mentally incompetent or unable to understand what participation to the study entails, a known alcohol or drug abuser, and/or anticipated to be non-compliant).
- Patient has any condition, which in the judgement of the Investigator, may chemically skew bone marrow. This may include but is not limited to the following:
- Cancer
- Undergoing chemotherapy radiation,
- Bone marrow transplant
- Infection at the donor sites
- Organ transplant on antirejection meds
- Usage of anti-rheumatologic drugs
- Chronic steroid usage
- Anemia
- Myelodysplastic Syndromes
- Patient presents with arthritis of the knee and may require knee replacement within the next 12 months.
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Interventions
DEVICEAvitus Bone Harvester
Patients will receive standard of care treatment, in addition to one extra bone marrow sample obtained using the Avitus Bone Harvester.
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT07434505