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CompletedNCT07263633Updated Dec 4, 2025

Additive Versus Subtractive Manufacturing Techniques of Custom-Made Plates for the Fixation of Interforaminal Mandibular Fractures

An interventional study of additive plating group and subtractive plating group in Anterior Mandibular Fracture, sponsored by Tanta University. Completed at 1 site in Egypt. Open to participants aged 16 Years to 60 Years. Per ClinicalTrials.gov, last updated 2025-12-04.

Sponsored by Tanta University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 10 months after the study started (first participant enrolled Dec 2024, registered Nov 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
16
Allocation
Randomized
Ages
16 Years to 60 Years
Sex
All
01

Study summary

This study aims to compare the mechanical properties, including tensile strength, shear strength, and flexural strength, as well as the clinical outcomes of additive and subtractive manufacturing techniques used to fabricate custom-made plates for the fixation of interforaminal mandibular fractures. A total of 16 patients were included and allocated into two groups: one treated using plates fabricated with the additive manufacturing technique and the other with the subtractive manufacturing technique. Mechanical performance was evaluated using standardized biomechanical testing, while clinical outcomes were assessed during scheduled postoperative follow-up visits. The objective of the study is to determine which fixation approach provides superior biomechanical performance and favorable clinical healing outcomes.

Read the detailed description

This randomized clinical study included 18 patients who were assessed for eligibility. Two patients were excluded-one did not meet the inclusion criteria and another declined participation-leaving a final sample of 16 patients who were randomly allocated into two equal groups (n=8 per group). All included patients were followed throughout the entire study period, and none were lost to follow-up.

Both study groups demonstrated comparable baseline characteristics with no statistically significant differences regarding age, sex distribution, trauma side, cause of injury, type of fracture, and operative time. All surgical procedures were performed using standardized operative protocols, and postoperative evaluations were conducted at fixed intervals.

Clinical outcomes included wound healing status, postoperative edema, infection, and wound dehiscence. Functional performance was evaluated through maximum mouth opening measurements and patient-reported outcomes involving occlusion and self-chewing ability. Radiographic and mechanical assessments were also performed, including tensile strength, shear strength, and flexural bending tests for the fixation systems used in each group.

Across the follow-up period, both groups showed satisfactory wound healing, absence of infection or dehiscence, progressive improvement in mouth opening, and gradual restoration of occlusal stability and chewing function, with no significant intergroup differences in clinical parameters. Mechanical testing demonstrated significant differences between the two fixation systems.

All collected data were statistically analyzed, and outcomes were reported in accordance with CONSORT guidelines.

02

Conditions studied

  • Anterior Mandibular Fracture

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Keywords

  • Additive
  • Subtractive
  • Custom-Made Plates
  • Interforaminal
  • Mandibular
  • Fractures
03

In context

Fractures, Bone

2,261 studies on the registry are indexed under Fractures, Bone; 325 are open to participants now.

This study's enrollment of 16 is below the median of 69 across 1,482 interventional studies indexed under Fractures, Bone.

Browse Fractures, Bone studies →

Lead sponsor

Tanta University is the lead sponsor of 963 studies on the registry; 304 are open to participants now.

Of its 16 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
16 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Isolated or non-isolated mandibular fractures located between the mental foramina (interforaminal fractures).

Exclusion criteria

Exclusion Criteria:

  • Patients with relevant systemic diseases that affect bone healing.
  • Comminuted fractures in which it is difficult to fix.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
16 participants (actual)

Study arms

  • Experimental
    additive plating group

    Additive manufacturing typically describes any process where material is gradually added, layer by layer, to form a final product. The term is often used interchangeably with 3D printing and rapid prototyping, although rapid prototyping can also involve other techniques beyond additive methods

    Device: additive plating group

  • Active comparator
    subtractive plating group

    In subtractive manufacturing, objects are created by progressively removing material from a solid block or sheet through processes such as cutting, drilling, boring, or grinding. While these processes can be performed manually, they are more commonly executed using computer numeric control (CNC). CNC machining is the most widely used subtractive manufacturing process today

    Device: subtractive plating group

Interventions

  • Deviceadditive plating group

    Additive manufacturing is the process of creating parts by joining materials based on 3D model data, typically layer by layer, in contrast to subtractive and formative manufacturing methods. While most of the global activity in additive manufacturing currently involves polymer-based systems, there has been increasing interest and activity in fabricating metallic parts

  • Devicesubtractive plating group

    In CNC machining, cutting tool removes material to achieve the desired geometry. The process involves using CAD to create the model to be machined and CAM to provide instructions to the CNC machine on how to remove the material. There are three major machining processes for material removal based on 3D models: turning, drilling, and milling. Additional subtractive manufacturing techniques, such as laser cutting, waterjet cutting, electrical discharge machining, and plasma cutting, are typically used for 2D machining

06

What researchers measure

Primary outcomes

  1. Tensile Strength

    Tensile strength will be measured using a universal testing machine (Instron) to evaluate the resistance of each plate to tensile forces according to standardized biomechanical testing protocols. Unit of Measure: Newton (N) Measurement Tool: Instron Universal Testing Machine.

    Time frame: After fabrication of the plates (baseline biomechanical assessment)

  2. Shear Strength

    Shear strength will be tested using the Instron universal testing machine to determine the resistance of the plate to shear loading. Time Frame: After fabrication of the plates (baseline biomechanical assessment) Unit of Measure: Newton (N) Measurement Tool: Instron Universal Testing Machine.

    Time frame: Immediately after fixation (within 24 hours)

  3. Outcome Measure

    Title: Overall Mechanical Stability Description: Overall biomechanical stability will be evaluated based on combined tensile, shear results. Time Frame: Within 24 hours after surgical fixation Unit of Measure: Stability index (unitless)

    Time frame: Immediately after fixation (within 24 hours)

Secondary outcomes

  1. Mouth Opening Measurement

    Maximum inter-incisal distance will be measured using a digital caliper to assess functional recovery and detect any restrictions. Unit of Measure: Millimeters (mm) Measurement Tool: Digital caliper

    Time frame: 1 week, 2 weeks, 1 month, 3 months, and 6 months after surgery

  2. Wound Healing Score

    Wound healing will be assessed using the Landry, Turnbull, and Howley Wound Healing Index, which evaluates tissue color, bleeding on palpation, granulation tissue, and overall appearance. Unit of Measure: Score (0-5 scale) Measurement Tool: Landry, Turnbull \& Howley Index (clinical scale)

    Time frame: 1 week, 2 weeks, 1 month, 3 months, and 6 months after surgery

  3. Postoperative Edema Measurement

    Edema will be measured using standardized linear facial measurements (tragus-pogonion and gonion-pogonion distances) to quantify postoperative swelling. Unit of Measure: Millimeters (mm) Measurement Tool: Facial linear measurement with ruler/caliper.

    Time frame: 1 week, 2 weeks, 1 month, 3 months, and 6 months after surgery

  4. Postoperative Infection Assessment

    Infection will be evaluated using the CDC Surgical Site Infection (SSI) criteria, including redness, swelling, warmth, purulent discharge, fever \>38°C, and localized tenderness at the surgical site.Unit of Measure: Presence or absence (Yes/No) Measurement Tool: CDC SSI Diagnostic Criteria (clinical assessment)

    Time frame: 1 week, 2 weeks, 1 month, 3 months, and 6 months after surgery

07

Study locations

1 site
  • Faculty of Dentistry, Tanta University
    Tanta, Gharbia Governorate 31527, Egypt
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 4, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07263633
Lead sponsor
Tanta University
Responsible party
FARIS INAD S ALANAZI (Principal Investigator, Master's Student, Department of Oral and Maxillofacial Surgery, Faculty of Dentistry, Tanta University, Tanta University) — Principal investigator
First posted
Dec 4, 2025
Start date
Dec 28, 2024
Primary completion
Jul 30, 2025
Completion
Oct 29, 2025
Last update
Dec 4, 2025

Study contacts

FARIS I ALANAZI
principal investigator · Faculty of Dentistry, Tanta University
Rafic R Bedir
principal investigator · Faculty of Dentistry, Tanta University
Ahmed G Abushahba
principal investigator · Faculty of Dentistry, Tanta University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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