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NCT Number: NCT07231042

Evaluation of Accuracy of Patient-Specific Plate for Reduction and Fixation of Mandibular Angle Fracture

This study evaluates the accuracy and clinical effectiveness of patient-specific titanium plates designed using CAD/CAM technology for the reduction and fixation of mandibular angle fractures. The customized plates are manufactured to match each patient's anatomical morphology, aiming to improve surgical precision, minimize operative time, and enhance postoperative stability. The study assesses clinical outcomes including pain, edema, occlusion, sensory recovery, maximal mouth opening, and radiographic bone healing across multiple follow-up periods. The goal is to determine whether patient-specific plates offer superior clinical and radiographic results compared with conventional fixation methods.

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Key information

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Faculty of Dentistry, Tanta University

Tanta, Gharbia Governorate, 31527, Egypt

About this study

This clinical study investigates the use of computer-aided design and computer-aided manufacturing (CAD/CAM) technology to fabricate patient-specific titanium plates for the reduction and fixation of mandibular angle fractures. The customized plates are created based on each patient's CT-derived anatomical morphology, allowing the surgical team to perform virtual planning, simulate fracture reduction, and generate an accurately fitted plate prior to surgery.

The primary objective of the study is to assess the accuracy of anatomical reduction achieved using patient-specific plates and to evaluate short- and medium-term clinical outcomes. All patients are treated using an intraoral surgical approach, with fracture reduction performed according to the preoperative virtual plan. The patient-specific titanium plate is then positioned and fixed without the need for intraoperative plate bending.

Clinical outcomes evaluated in this study include postoperative pain, facial edema, maximal mouth opening, sensory recovery of the inferior alveolar nerve, dental occlusion, and wound healing. Radiographic assessment evaluates bone healing, alignment, intergonial distance, and the accuracy of fracture reduction across multiple follow-up intervals. These evaluations aim to determine the stability and precision of the patient-specific fixation method.

The study follows patients through standardized follow-up periods, including immediate postoperative assessment, 1-week, 1-month, 3-month, and 6-month evaluations. Data are collected prospectively using unified clinical forms and radiological imaging protocols. All procedures adhere to ethical guidelines, and informed consent is obtained from all participants prior to enrollment.

The rationale behind using patient-specific plates is the potential to improve biomechanical stability, reduce operative time, eliminate intraoperative plate bending, and achieve more predictable postoperative outcomes. This study aims to provide evidence on whether CAD/CAM-based customized plates offer measurable advantages over conventional fixation systems in the treatment of mandibular angle fractures.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patient with displaced mandibular angle fracture indicated for open reducation and internal fixation.
  • Age of patient > 18 years old .

Exclusion criteria

1- Medically compromised patients with impaired healing ability.

Treatment and study plan

Patient-Specific Titanium Plate

Device

A customized titanium fixation plate designed using computer-aided design and manufacturing (CAD/CAM) technology based on preoperative CT data. The plate is fabricated to precisely match the patient's mandibular anatomy and used for open reduction and internal fixation of mandibular angle fractures.

Primary outcomes

  1. Accuracy of Fracture Reduction

    Time frame: Immediately and 1 week postoperatively

    Accuracy of anatomical reduction will be evaluated by comparing postoperative CBCT scans with preoperative virtual surgical plans using superimposition analysis to measure the deviation between planned and achieved fragment positions.

Secondary outcomes

  1. Postoperative Pain Intensity

    Time frame: 1 day, 1 week, and 1 month postoperatively

    Pain intensity will be recorded using a Visual Analogue Scale (VAS) ranging from 0 (no pain) to 10 (worst pain).

  2. Postoperative Facial Edema

    Time frame: 1 week and 2 weeks postoperatively

    Facial swelling will be measured using the Souza JA facial edema scale based on standardized anthropometric landmarks.

  3. Occlusal Relationship and Stability

    Time frame: 1 week, 1 month, and 3 months postoperatively

    Occlusal stability will be evaluated clinically using the Uglešić occlusion score to assess the degree of alignment and functional contact between opposing teeth

  4. Recovery of Inferior Alveolar Nerve Function

    Time frame: 1 week, 1 month, and 3 months postoperatively

    Sensory recovery of the lower lip and chin will be assessed using light touch and two-point discrimination tests

  5. Radiographic Bone Healing

    Time frame: 3 and 6 months postoperatively

    Bone union and callus formation will be assessed radiographically on CBCT images to confirm complete healing and stability at the fracture site.

Sponsors and collaborators

Lead sponsor

Tanta University

Other

Registry information

Official study title

Evaluation of Accuracy of Patient Specific Plate for Reduction and Fixation of Mandibular Angle Fracture

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Nov 17, 2025
Registry last updated
Nov 17, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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