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Facial FractureNCT03292679

Craniofacial Applications of 3D Printing

An observational study of Facial Fracture, run by University of Maryland, Baltimore at 1 site in United States.

Withdrawn

Withdrawn. The study stopped before anyone enrolled.

Official record
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Trial summary

3D printing is a technology that allows for physical creation of a 3D model (usually made of plastic) based on computer generated 3D images from CT scans. The 3D images of craniofacial skeleton using computer software are routinely generated and, in turn, these 3D images can be used to create a plastic 3D model using… Read more about this study

Who is it for?
Ages 12 years and older
Conditions the study is for
Facial Fracture
What is being tested?
3D template
Type of treatment
Surgery or procedure
How many people
0 participants
Where
1 siteUnited States
Study dates
Jun 2019to Sep 2020
How long will I take part?
1 Year
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 12 years and older
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

Study population: Patients presenting to Shock Trauma Plastic Surgery Division for treatment of facial fractures

Who may be able to join

  • Patients with face CT scans
  • Patients with facial fractures
  • Patient age 12 years or older

Who cannot join

  • Patients without CT scan
  • Patients with facial fractures that do not require rigid fixation using hardware
  • Patients with facial fractures that do not have normal contralateral bony structures
  • Patient age less than 12 years

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Arthur J Nam

    Baltimore, Maryland, 21201

Other trials in United States

About this study

3D printing is a technology that allows for physical creation of a 3D model (usually made of plastic) based on computer generated 3D images from CT scans. The 3D images of craniofacial skeleton using computer software are routinely generated and, in turn, these 3D images can be used to create a plastic 3D model using a 3D printer.

Unstable or comminuted facial fractures need to be reduced and rigidly fixated using titanium plates and screws. Bending and shaping of the plates is usually performed by free-hand based on the surgeon's estimation of what best fits the fracture.

Read more

Often, bending the titanium plates to the shape of pre-injury skeletal contour is difficult when the bone is fractured into many pieces or is unstable, or when the patient is edentulous (missing several teeth). The process can increase the time spent in surgery and the bent plates may not snugly fit the fracture. For these difficult cases, one option is to use commercially manufactured 3D printed patient-specific models. The patient-specific models provide the benefit of correct shape / form for increased surgical accuracy, and decreased intra-operative time. However these commercial models are manufactured at distant facilities and usually require more than 7 days before delivery. As such, they delay time to surgery and cannot be used for urgent surgery. Additionally, the commercially manufactured implants are expensive, significantly increasing the cost of treatment.

The purpose of this study is to explore whether custom plastic models 3D printed at Shock Trauma Center and used for bending and shaping plates for facial fracture repair can improve results of facial fracture reconstruction.

Our plastic surgery division will design and produce facial bone 3D model of patients (with facial fractures) using an in-house 3D printer, then use the 3D model to contour the hardware pre-op or intra-op at the time of fracture repair. We believe that we can achieve better repair, shorter surgery time, and save hardware cost.

Read the detailed description

The purpose of this study is to:

  1. produce 3D printed craniofacial models of patients with facial fracture, then use the 3D models
  2. contour (or pre-bend) the appropriate hardware pre-op that is specific for the patient.

Fracture repair in the operating room entails exposure and reduction of the fracture, followed by contouring the hardware to the correct shape to maintain the fracture reduction. However, in unstable or comminuted fractures or in patients missing several teeth, contouring the plate to the correct shape can be time consuming and, sometimes, the plate shape can be inaccurate. Our hypothesis is that using our own 3D model printed on-site to "pre-bend" plates will save intra-operative time and cost, and achieve superior clinical outcome.

Patients will be enrolled to participate if they meet inclusion and exclusion criteria, and provide informed consent.

Additionally, for study subjects, protected health information such as name, date of birth, medical record number, and demographic information (age, sex, ethnic group), Billing and payment information with medical justification, clinical information related to the procedure and follow-up visits will be handled by research personnel for research purposes.

Otherwise, management of the study subjects will be essentially the same as for patients that are not enrolled in the study. This includes CT scans obtained postoperatively to confirm adequate fracture repair, routine clinic follow-up visits (during post-op week 1, week 4, 3 months, 6 months, and/or 1 year after surgery) and additional follow-up visits as may be deemed necessary based on clinical status.

Prior experience of utilizing on-site 3D printing technology in facial reconstruction surgery is limited. If a patient-specific plate is needed, then the plates must be made by commercial manufacturers which usually takes days to produce, and is therefore not suited to treatment of facial trauma.

Trauma plastic surgery division owns and operates a 3D printer. We have experience with CT image processing and have made 3D models of patients facial skeleton (i.e. midface, mandible) that were used as templates for repairing facial fractures.

Patients with complex facial injuries or defects require reconstruction using hardware to restore facial contour and functional stability. In many complex facial reconstructions, surgeons consult commercial companies for expertise in computer aided design and manufacturing of patient-specific implants. The advantages of undergoing this process include (1) in-depth anatomic analysis, (2) improved design of hardware leading to better surgical outcome, and (3) shortened OR time. The disadvantages include length of time required for the production of patient-specific implant (usually 3 to 7 days), and high cost: for example, a mandible 3D model and associated patient-specific reconstruction plate is >$3000.

Three-dimensional printing is an actively evolving technology, especially in surgery. Design modifications and improvement in extrusion technology have made 3D printing made this process much more affordable and relatively easy. It is now possible for individuals (and surgeons!) to generate these 3D models.

Repair of mandible fractures is especially challenging when the patient is edentulous (missing several or all teeth) for several reasons including the smaller bulk of the edentulous mandible, requiring larger reconstructive plates spanning a bigger section of the jaw. Surgery generally takes longer for these patients when compared with non-edentulous patients. A substantial portion of the lengthiness is due to time spent bending the plate.

The rationale for this IRB proposal is to explore the efficacy of 3D models of the patient's fracture that are printed in house as aids for facial fracture reconstruction. We hypothesize that reconstruction with the aid of the models will require shorter OR time, improve bony fixation, without significant increase in overall cost of treatment.

Conditions
Facial Fracture
Being tested
3D template

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • 3D templateProcedure or surgery

    A 3D-printed model of relevant portions of the patient's facial skeleton, based on patient's CT scan will be created. This model will be used to bend titanium reconstruction plates that are used to stabilize the facial fracture for subjects in the treatment group.

    Bending of the plates will be performed in the operating room during the patient's surgery. Titanium reconstruction plates are used to stabilize the fracture whether or not the individual is in the study. However, for patients that are in the treatment arm of the study, the plates are bent with the aid of the 3D-printed model as template, rather than by free-hand.

Study groups in NCT03292679
Study groupRoleWhat they receive
3D templateSubjects will have custom models of relevant portions of their facial skeleton printed and used as templates for bending and shaping plates for stabilizing the fracture(s).
Receives: Procedure: 3D template

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Operative time

    Duration of fracture fixation

    Measured: 24 hours

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted25 Sep 2017
  2. Study startJun 2019 (estimated)
  3. Primary completionSep 2020 (estimated)
  4. Study completionSep 2020 (estimated)

Why it stopped: There was lack of internal staff support and could not enroll participants.

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
0 participants (actual)
Target duration
1 Year
IDs, dates and publications
ClinicalTrials.gov ID
NCT03292679
Sponsor's protocol ID
HP-00071854
Status last verified
Mar 2023
First submitted
20 Sep 2017
Last updated
3 Apr 2023
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Facial Fracture, run by University of Maryland, Baltimore at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: withdrawn, as of the sponsor's last update on 3 Apr 2023. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study was withdrawn before enrolling participants, so there are no results.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Operative time (time frame: 24 hours). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 3 Apr 2023.

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