Condition: Bone Graft; Complications · ACL Injuries · Sponsor: University of Arizona
All patients will be randomly assigned using a computer randomization algorithm to one of two matched cohort groups. Patients will not be advised which group they belong to until after the completion of the study. One group will be treated with autologous bone graft for bone patellar-tendon bone (BTB) Anterior Cruciate Ligament Reconstruction (ACLR), and the other group will be treated with commercially available DBM (Demineralized bone matrix) putty. Patients will be enrolled from Banner University. Before and after surgery, patient reported outcomes including visual analog pain scale (VAS), Tegner-Lysholm and Cincinnati ACL Test. The principal investigator will evaluate the patients on subjective criteria such as pain and objective criteria including range of motion, arthritic changes seen on radiographs, infection, and ability to kneel.
This description comes directly from the study's public registry record.
Marleny Munoz · 602-793-9582 · marlenymunoz@arizona.edu
Phoenix Biomedical Campus Regulatory Team · mlburchfi@arizona.edu
Always discuss trial participation with your own doctor first.
| Banner University Medical Center Phoenix | Phoenix, Arizona, United States | Recruiting |
| Banner Health Center Plus - Arcadia | Phoenix, Arizona, United States | Recruiting |
| Banner Sports Medicine Scottsdale | Scottsdale, Arizona, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06975306