Clinical Assessment of Computer-assisted PEEK Versus Conventional Titanium Plates on Mandibular Body Fractures

Sponsor
Cairo University (Other)
Overall Status
Unknown status
CT.gov ID
NCT03466190
Collaborator
(none)
20
1
2
19
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Study Details

Study Description

Brief Summary

Two groups of patients with mandibular body fractures indicated for Open reduction internal fixation alone or in combination with fractures elsewhere in the mandible or midface. First group will be subjected to traditional titanium internal rigid fixation. Second group will be subjected to custom made PEEK plates.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Titanium plate fixation
  • Procedure: Custom made PEEK plate fixation
N/A

Detailed Description

Two groups of patients with mandibular body fractures indicated for Open reduction internal fixation alone or in combination with fractures elsewhere in the mandible or midface. First group will be subjected to traditional titanium internal rigid fixation. Second group will be subjected to custom made PEEK plates.

Inclusion criteria:
All subjects were required:
  1. Patients with at least a unilateral body fracture indicated for Open reduction internal fixation alone or in combination with fracture elsewhere in the mandible or midface.

  2. All ages and both sexes were included in this study.

  3. Patients should be free from any systemic disease that may affect normal healing of bone, and predictable outcome.

  4. Patients with good general condition allowing major surgical procedure under general anesthesia.

  5. Patients with physical and psychological tolerance.

Exclusion criteria:
  1. Patients with high risk systemic diseases like uncontrolled diabetes . As uncontrolled diabetes has a negative impact on normal bone healing.

  2. Patients with old fractures. As they will affect accuracy of reduction of the fractured segments.

  3. Patients with physical and psychological intolerance. As psychological stress will affect the immune system and patient's fitness including healing capacity.

Interventions:

Eligible patients will be randomized in equal proportions between the study group (PEEK custom made plates) and the control group (titanium plates).

A- Computer-assisted PEEK custom made plates:
  • All cases will undergo surgery under general anesthesia.

  • Exposure of the fractured segments will be done using a standardized surgical approach.

  • The fractured segments will be reduced in normal anatomic position guided by customized plate.

  • Fracture fragments will be fixed using PEEK custom made plate utilizing 2.0 mm screws.

B- Conventional titanium plates:
  • All cases will undergo surgery under general anesthesia.

  • Exposure of the fractured segments will be done using a standardized surgical approach.

  • Inter-maxillary fixation will be done.

  • The fractured segments will be reduced in normal anatomic position guided by occlusion.

  • The fracture fragments will be fixed using 2.3 titanium plate on the inferior border and 2.0 titanium plate on the superior border utilizing bone screws.

Follow up:

Clinical evaluation will be performed at the first week postoperative. Computed tomography will be performed at the first week postoperative then patients will be recalled for clinical evaluation every week for one month. Final follow up visit will be at 3 months postoperative.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
20 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
A Randomized clinical trial. A trial will be carried out in hospital of Oral and Maxillofacial surgery department- Faculty of Oral and Dental Medicine Cairo University Equal randomization: participants with equal probabilities for intervention. Positive controlled: Both groups receiving treatment. Parallel group study: Each group of patients receives a single treatment simultaneously.A Randomized clinical trial. A trial will be carried out in hospital of Oral and Maxillofacial surgery department- Faculty of Oral and Dental Medicine Cairo University Equal randomization: participants with equal probabilities for intervention. Positive controlled: Both groups receiving treatment. Parallel group study: Each group of patients receives a single treatment simultaneously.
Masking:
None (Open Label)
Masking Description:
Because the two interventions used in this trial are clearly different and easily recognized by the participants and investigators, neither the investigator nor participants can be blinded
Primary Purpose:
Treatment
Official Title:
Clinical Assessment of Postoperative Occlusion in Patient With Mandibular Body Fractures Reduced and Fixed With Computer-assisted Polyether Ether Ketone (PEEK) Custom Made Plates Versus Conventional Titanium Plates (RCT)
Actual Study Start Date :
Aug 2, 2017
Anticipated Primary Completion Date :
Mar 2, 2019
Anticipated Study Completion Date :
Mar 2, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: Custom made PEEK plate fixation

Open Reduction Internal Fixation using Custom made PEEK plates.

Procedure: Custom made PEEK plate fixation
Under General Anesthesia, exposure of the fractured mandibular body segments will be done using a standardized surgical approach. Open Reduction Internal Fixation using custom made PEEK plates will be performed.
Other Names:
  • Computer-assisted PEEK plate fixation
  • Active Comparator: Titanium plate fixation

    Open Reduction Internal Fixation using conventional titanium plating system.

    Procedure: Titanium plate fixation
    Under General Anesthesia, exposure of the fractured mandibular body segments will be done using a standardized surgical approach. Open Reduction Internal Fixation using conventional titanium plates will be performed.
    Other Names:
  • Conventional titanium plates
  • Outcome Measures

    Primary Outcome Measures

    1. Postoperative occlusion [1 month postoperative]

      Restoration of normal patient occlusion will be assessed using Visual analog scale (VAS) (0-10)

    Secondary Outcome Measures

    1. Accuracy of the planned reduction [1st week]

      The accuracy of computer assisted PEEK custom made plates in open reduction and internal fixation of mandibular body fractures will be assessed using Mimics software, measuring unit (mm)

    2. Wound dehiscence [1 month postoperative]

      Wound infection will be assessed via clinical assessment, measuring unit (Binary yes/no)

    3. The need for 2nd surgery [1 month postoperative]

      Redo surgery will be assessed via clinical assessment, measuring unit (Binary yes/no)

    4. Operative time [During operation]

      Surgical time will be assessed via clinical assessment, measuring unit (hours)

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. Patients with at least a unilateral body fracture indicated for Open reduction internal fixation alone or in combination with fracture elsewhere in the mandible or midface.

    2. All ages and both sexes were included in this study.

    3. Patients should be free from any systemic disease that may affect normal healing of bone, and predictable outcome.

    4. Patients with good general condition allowing major surgical procedure under general anesthesia.

    5. Patients with physical and psychological tolerance.

    Exclusion Criteria:
    1. Patients with physical and psychological intolerance. Because psychological stress will affect the immune system and general health.

    2. Patients with systemic diseases like uncontrolled diabetes mellitus. Because uncontrolled diabetes mellitus has a negative impact on normal bone healing.

    3. Patients with old and/or mal-union fractures. As they will affect accuracy of reduction of the fractured segments.

    4. Patient with bad oral hygiene. As it has an influence on normal osseous healing

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Faculty of Oral and Dental Medicine -Cairo University Cairo Giza Egypt 12613

    Sponsors and Collaborators

    • Cairo University

    Investigators

    • Study Director: Khaled Amr, PhD, Faculty of Oral and Dental Medicine -Cairo University

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    Rofaida Atef Atef, Assistant lecturer, Cairo University
    ClinicalTrials.gov Identifier:
    NCT03466190
    Other Study ID Numbers:
    • CEBD-CU-2018-02-27
    First Posted:
    Mar 15, 2018
    Last Update Posted:
    Mar 15, 2018
    Last Verified:
    Mar 1, 2018
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Rofaida Atef Atef, Assistant lecturer, Cairo University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 15, 2018