Bone Graft Clinical Trials

Clinical trials related to Bone Graft Procedure

Comparison of Iliac Crest Marrow vs. Proximal Tibia Avitus® Bone Graft

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
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
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 70
Healthy Volunteers: f
View:

• 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.

Locations
United States
Florida
Mayo Clinic
RECRUITING
Jacksonville
Contact Information
Primary
Edward T Haupt, M.D.
Haupt.Edward@mayo.edu
904-953-2496
Time Frame
Start Date: 2025-11-06
Estimated Completion Date: 2026-12
Participants
Target number of participants: 12
Treatments
Experimental: Autograft Bone Harvest
Patients undergoing an orthopedic foot and ankle surgery in which an autograft bone harvest will be performed.
Related Therapeutic Areas
Sponsors
Leads: Mayo Clinic
Collaborators: Zimmer Biomet

This content was sourced from clinicaltrials.gov