About this trial
This project consists of a prospective case design. Study candidates will include all patients ages 18 and over who were evaluated at UCSD and found to have a critical-sized humerus, femur, or tibia segmental defect that would be fixed through surgery. Patients who consent to study participation will receive the TRUMATCH Graft Cage for their long bone segmental defect repair. Data on healing rates, complication rates, re-operation rates, time to return to normal activity, and pain levels will be collected for each participation. After 3 years of data collection, we will analyze this data to provide further insight on the utility of the TRUMATCH Graft Cage. Given the significant difficulty with repairing segmental long bone defects, it is imperative to evaluate novel systems to appropriately manage these injuries.
Eligibility criteria
Qualifiers
Humerus, femur, or tibia segmental defects requiring surgery
Evaluation and treatment at UCSD
Ages 18 year and older
Abiltiy to understand the content of the patient information/informed consent form
Disqualifiers
Any not medically managed severe systemic disease
Their doctor has decided that it is in the patient's best interest to receive a different method of repair
Their doctor has determined that the patient has a condition that would make them unsuitable for participation in the study
Pregnancy or women planning to conceive within the subject participation period (1 year) note: pregnancy will be self-reported and no test will be performed to test for it
Trial design
Treatments tested in this trial
- TRUMATCH Graft Cage