About this trial
This project focuses on patients with chest wall tumors who are expected to have a maximum intraoperative anterolateral chest wall defect diameter of 5-10 cm and require chest wall reconstruction with rib implants. It aims to evaluate the efficacy and safety of biodegradable 3D-printed implants in chest wall reconstruction surgery, providing a superior reconstruction strategy for patients with tumor-induced chest wall defects.
Eligibility criteria
Qualifiers
Aged 18-70 years;
No gender restriction;
ECOG Performance Status 0-1;
Chest CT-confirmed chest wall-originating tumor;
Disqualifiers
Patients with posterior chest wall defects;
Uncontrolled underlying medical conditions or contraindications to general anesthesia;
Pregnant or lactating women;
Concurrent severe comorbidities that may interfere with study evaluations, including: Severe hepatic, cardiac, or renal diseases; Active malignancies (other than the indicated chest wall tumor); Alcohol use disorder
Trial design
Treatments tested in this trial
- Chest wall reconstruction