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3D Printed Models for Mandibular Fracture Repair

Primary Purpose

Mandible Fracture, Maxillofacial Trauma

Status
Not yet recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
3D Printed Model
Sponsored by
University of Cincinnati
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Mandible Fracture focused on measuring 3D Printing, Personalized Medicine, Maxillofacial Trauma

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Patient ≥ 18 years of age Patients who have received either a cone beam or conventional CT Admitted through University of Cincinnati Hospital and Medical Center emergency department All isolated mandible fractures referred to University of Cincinnati Hospital Oral & maxillofacial surgery clinic Surgical team members from the division of plastic and otolaryngology Exclusion Criteria: Patient < 18 years of age Patients who have neither cone beam nor conventional CT Patients requiring a repeat procedure Unexpected exposure of hardware

Sites / Locations

  • University of Cincinnati Medical Center
  • UC Health Holmes Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

3D Model Generated

Normal Standards of Care without Aide of Model

Arm Description

Patient will undergo an Open Reduction and Internal Fixation preformed by a surgeon who had pre-operative access to a 3D model printed to help pre-bend hardware.

Patient will undergo standard Open Reduction and Internal Fixation by a surgeon who did not have a pre-operative 3D model.

Outcomes

Primary Outcome Measures

Total time in the OR
Time in the OR considered critical part of the procedure by the Oral & Maxillofacial Surgery Staff
Subjective outcome to surgeon
Surgeon overall satisfaction with utilizing the 3D generated model, obtained via Likert Scale Questions completed post-operatively. The investigators are going to use the Likert questions to develop a numerical scoring system and report that data as "raw" Likert scores. Likert questions and conversion of specialists' responses to Anatomic Model Utility Points (AMUPs). Responses of "strongly disagree", "disagree", and "neutral" were assigned 0 AMUP points. Responses to preprocedural confidence are assigned negative points, to effectively subtract the impact of the anatomic model post- versus pre-procedure. The maximum AMUP for each patient was 500.

Secondary Outcome Measures

Full Information

First Posted
January 10, 2023
Last Updated
February 14, 2023
Sponsor
University of Cincinnati
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1. Study Identification

Unique Protocol Identification Number
NCT05733221
Brief Title
3D Printed Models for Mandibular Fracture Repair
Official Title
Determining the Ease of Utilizing 3D Printed Models to Aide in Isolated Mandibular Fracture Repair
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
March 2023 (Anticipated)
Primary Completion Date
February 2024 (Anticipated)
Study Completion Date
April 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Cincinnati

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Data Monitoring Committee
No

5. Study Description

Brief Summary
The investigators will test the hypothesis that patients randomized to the intervention (3D printing with pre-bent plate) arm have less operative room time and less time for the critical part of the procedure than patients in the control arm (no 3D printing, current standards of care). Personalized medicine and care for fracture treatment.
Detailed Description
The goal of treatment is to re-establish the patient's preinjury dental occlusion and facial harmony. Fractures that are nondisplaced and exhibit no occlusal changes may be amenable to nonsurgical management, but most mandible fractures will require stabilization for satisfactory healing and to restore pretraumatic maxillomandibular orientation. Various treatment strategies have been described and vary widely depending on the fracture location and surgeon's preference. The patient's demographics, comorbidities, dentition, and fracture characterization will all influence the choice of fixation by the treating surgeon. There are very few randomized control trials that show outcomes when 3D printing is used for intervention planning and performing a procedure. These data are essential to establish value of 3D printing as a clinical service. There is also anecdotal evidence that a 3D printed model of a mandible fracture can be useful for pre-operative planning because the oral and maxillofacial surgeon can better assess the geometry of the bone lesions and can pre-bend fixation plates before the procedure. This hypothetically decreases the amount of time in the operating room. The investigators propose a parallel design randomized control trial to study the value of 3D printing for preoperative planning in patients with a fracture of the mandible who require open reduction, internal fixation. The study will be split into two arms: 1) Patients that will have a 3D model generated for the surgical procedure 2) The control group who will follow normal standards of care as outlined above and won't have the additional 3D model created pre-operatively.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mandible Fracture, Maxillofacial Trauma
Keywords
3D Printing, Personalized Medicine, Maxillofacial Trauma

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The investigators propose a parallel design randomized control trial to study the value of 3D printing for preoperative planning in patients with a fracture of the mandible who require open reduction, internal fixation. The study will be split into two arms: 1) Patients that will have a 3D model generated for the surgical procedure 2) The control group who will follow normal standards of care as outlined above and won't have the additional 3D model created pre-operatively.
Masking
Participant
Masking Description
Once the subjects are identified the research coordinator will conduct a screening of the patient to ensure they meet the inclusion/ exclusion criteria for the study and then randomize the patient into either normal standard of care for surgical repair of the fractured mandible or normal standard of care for surgical repair of the fractured mandible aided by a 3D printed model of the patient's jaw.
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
3D Model Generated
Arm Type
Experimental
Arm Description
Patient will undergo an Open Reduction and Internal Fixation preformed by a surgeon who had pre-operative access to a 3D model printed to help pre-bend hardware.
Arm Title
Normal Standards of Care without Aide of Model
Arm Type
No Intervention
Arm Description
Patient will undergo standard Open Reduction and Internal Fixation by a surgeon who did not have a pre-operative 3D model.
Intervention Type
Device
Intervention Name(s)
3D Printed Model
Intervention Description
3D Printed Model generated pre-operatively of the patients mandible.
Primary Outcome Measure Information:
Title
Total time in the OR
Description
Time in the OR considered critical part of the procedure by the Oral & Maxillofacial Surgery Staff
Time Frame
Total procedural time
Title
Subjective outcome to surgeon
Description
Surgeon overall satisfaction with utilizing the 3D generated model, obtained via Likert Scale Questions completed post-operatively. The investigators are going to use the Likert questions to develop a numerical scoring system and report that data as "raw" Likert scores. Likert questions and conversion of specialists' responses to Anatomic Model Utility Points (AMUPs). Responses of "strongly disagree", "disagree", and "neutral" were assigned 0 AMUP points. Responses to preprocedural confidence are assigned negative points, to effectively subtract the impact of the anatomic model post- versus pre-procedure. The maximum AMUP for each patient was 500.
Time Frame
Up to 2 days post-procedure

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient ≥ 18 years of age Patients who have received either a cone beam or conventional CT Admitted through University of Cincinnati Hospital and Medical Center emergency department All isolated mandible fractures referred to University of Cincinnati Hospital Oral & maxillofacial surgery clinic Surgical team members from the division of plastic and otolaryngology Exclusion Criteria: Patient < 18 years of age Patients who have neither cone beam nor conventional CT Patients requiring a repeat procedure Unexpected exposure of hardware
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Deepak G Krishnan, DDS
Phone
513-584-2586
Email
deepak.krishnan@uc.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Reese R Triana, MPH
Phone
513-584-2094
Email
reese.triana@uc.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Deepak G Krishnan, DDS
Organizational Affiliation
University of Cincinnati
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Cincinnati Medical Center
City
Cincinnati
State/Province
Ohio
ZIP/Postal Code
45219
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Deepak G Krishnan, DDS
Phone
513-584-2586
Email
deepak.krishnan@uc.edu
First Name & Middle Initial & Last Name & Degree
Frank J Rybicki, MD, PhD
Phone
513-558-2100
Email
rybickfk@ucmail.uc.edu
First Name & Middle Initial & Last Name & Degree
Deepak G Krishnan, DDS
First Name & Middle Initial & Last Name & Degree
Frank J Rybicki, MD, PhD
First Name & Middle Initial & Last Name & Degree
Reese R Triana, MPH
Facility Name
UC Health Holmes Hospital
City
Cincinnati
State/Province
Ohio
ZIP/Postal Code
45220
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Deepak G Krishnan, DDS
Phone
513-584-2586
Email
deepak.krishnan@uc.edu
First Name & Middle Initial & Last Name & Degree
Frank J Rybicki, MD, PhD
Phone
513-558-2100
Email
rybickfk@ucmail.uc.edu
First Name & Middle Initial & Last Name & Degree
Deepak G Krishnan, DDS
First Name & Middle Initial & Last Name & Degree
Frank J Rybicki, MD, PhD
First Name & Middle Initial & Last Name & Degree
Reese R Triana, MPH

12. IPD Sharing Statement

Plan to Share IPD
No
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3D Printed Models for Mandibular Fracture Repair

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