Patient-specific Reconstruction Plate for Segmental Mandibular Defects

Alexandria University

Status: Enrolling

Conditions: Mandibular Resection; Mandibular Reconstruction; Mandibular Reconstruction* / Methods

Treatments: Device: Patient specific reconstruction plate

Study type: Interventional

Funder types: Other

Identifiers

NCT07320924

20-12-25/PSRP

Details and patient eligibility

About

The mandible's horseshoe-shaped anatomy makes the reconstruction of segmental defects a challenging procedure. Conventional reconstruction typically relies on alloplastic plates to bridge bony stumps; however, these require extensive intraoperative bending, often resulting in imperfect adaptation, press-to-contact fixation, and residual stresses that increase the risk of hardware fatigue and fracture. Recent advances in computer-aided design and manufacturing (CAD/CAM) and virtual surgical planning (VSP) have improved precision in maxillofacial reconstruction. Patient-Specific Reconstruction Plates (PSRP), developed from virtual planning and patient-specific anatomical data, offer a bespoke contour adaptation, predictable screw positioning, and elimination of press-fit deformation. This customization improves alignment, mechanical stability, and long-term outcomes.

Full description

The study aims to assess the clinical performance and morbidity rate of computer-guided PSRP in the management of mandibular segmental defects.

This prospective interventional clinical trial will be conducted on a total of 14 patients with a segmental mandibular defect, recruited from Alexandria University Teaching Hospital. All patients will be reconstructed using a PSRP alloplastic bridging plate, utilizing a preoperative virtual surgical planning and design. Patients will be evaluated clinically for the rate of morbidity and range of mandibular excursions. Furthermore, postoperative radiographic 3D analysis will evaluate the accuracy of the computer-guided procedure.

Enrollment: 14 estimated patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Patients with a segmental mandibular continuity defect, not involving the condyle.

2. Patients suffering from benign, locally invasive or malignant lesions that involving the lower border of the mandible.

3. Patients with recurrent lesions after resection.

4. Patients dealing with osteomyelitis or jaw osteonecrosis that is indicated for sequestrectomy.

   • Stage-III jaw osteonecrosis.

5. Patients with traumatic defects.

6. Patients with post-gunshot mandibular defects.

Exclusion criteria

1. Medically compromised patients contradict the operation.
2. Patients with segmental mandibular defects that require condylar process resection
3. Patients with lateral segmental mandibular defects involving the condyle that require reconstruction using an alloplastic total joint.
4. Patients with an active infection at the site of resection.

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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14 participants in 1 patient group

Patient specific reconstruction plate

Experimental group

Description:

patient with mandibular ablation defect managed with patient specific reconstruction plate

Treatment:

Device: Patient specific reconstruction plate