Accuracy of 3D Printed Maxillary Complete Dentures

August 2, 2018 updated by: Hadeer mohamed mohamed, Cairo University

Accuracy of 3D Printed Maxillary Complete Dentures Compared With Conventional Complete Dentures: Non-Randomized Control Trial

Conventional complete dentures have been used for almost a century as a treatment choice for edentulous patients, despite of their inaccuracy & dimensional changes during manufacturing. Recently, new manufacturing techniques like RP/3D printing (rapid prototyping) has progressed in the dental field including prosthodontics, does the 3D printed complete denture show more accuracy than conventional ones?

Study Overview

Detailed Description

Conventional complete dentures have been used as a clinically accepted prosthetic treatment for completely edentulous patients for almost a century. [1] One of its advantages is ability to customize teeth arrangement and to check each step of the preceding steps before the delivery stage.

Conventional complete dentures fabrication consist of several steps of recording, transferring, evaluating, and creating artificial substitutes for patient's teeth and gingiva which must be in harmony with patient's mouth and face. All this steps demand high experience, artistic, and skillful operator and technician.

However denture processing results in polymerization shrinkage of the resin (due to flask cooling), and distortion of the denture base (due to stress release after denture base removal from the stone cast), and decreasing the accuracy and denture adaptation. [2] These dimensional changes increase the gap between the denture base and underlying mucosa, resulting in an ill-fitting denture.[3] Denture adaptation and fitting plays a crucial role in complete denture retention (by physical means), stability, and patient comfort. [4]

Also, flask closure must be done under considerable pressure to ensure metal-to-metal contact between the halves of the flask to confine the resin inside the mold with no excess.[5] In addition to the inherent processing shrinkage and/or expansion properties of the acrylic resin.[6] Researchers tried to overcome these disadvantages by changing the technique of polymerization of the resin, by using of microwave energy, dry heat, and visible light.[7] But unfortunately researchers found that, Discrepancies in the base adaptation shown by several techniques are not easily corrected after complete denture processing.[8] Denture base adaptation to the stone cast is usually not satisfactory, especially in the midline section of the central portion of the posterior border.[9] To overcome the previous disadvantages computer aided manufacturing technology was applied to complete dentures. Some advantages of digitally fabricated complete dentures are 1) reduced number of patient visits; 2) superior strength and fit of dentures; 3) omitting multiple error-introducing steps such as impression, waxing, and casting.[10] 4) reduced cost for patient and clinician; 5) easy denture duplication (due to stored digital data); 6) standardization of clinical research on complete dentures and implant-retained overdentures.

To fabricate physical prototype (model) there are two different approaches: subtractive and additive manufacturing.

Subtractive manufacturing is based on milling the denture from a larger blank by a computer numeric controlled (CNC) machine. The input data for this method are principally from an optical or contact probe digitizer, which can only capture the external surface data of the anatomy and not the internal tissue surface of the object.

Although CAD/CAM dentures have many advantages compared to conventional ones, but the CAD/CAM protocol introduces additional steps (like scanning, software modeling, and milling) in the fabrication process that can lead to inaccuracies.[11] Another disadvantage of CAD/CAM is its inability to reproduce fine details by milling .[12] Additive manufacturing is the process that creates objects from 3D model data, in an additive layer by layer manner.[13] The additive systems used in dentistry are stereo-lithography, selective laser sintering or melting, and 3D printing.

The main advantage of additive technology is the ability to create minor details (undercuts, voids, complex internal geometries) in the proposed model. In addition to Incremental vertical object build-up, no material wastage, large objects produced, passive production (i.e., no force application), and ability to print multiple materials at the same time (in case of 3D printing). [15] A clinical study was done to compare the accuracy values of maxillary conventional heat-polymerized trial denture bases with those RR printed ones and the results were as follows: Mean deviation was (-0.0051mm), (SD, 0.19mm).[16]

In the same study authors used ratings from 100-mm VAS in 10 patients and 20 prosthodontists comparing conventional and RP methods and the results were as follows:

Patients comparing overall satisfaction: P=0.59, prosthodontists comparing overall satisfaction: P=0.87 The term selective laser sintering is used to describe the fabrication of a pattern from ceramics or polymers while selective laser melting describes pattern fabrication from metal.[14] The laser beam locally raises the temperature close to the melting point of the metal particle, to avoid complete melting. The platform is slightly immersed in the powder, and powder thickness is controlled by a cylinder rolling on the powder pool. After each new powder layer application, the laser melting process is repeated until the 3D object is completed.

Stereo lithography technology consists of photosensitive resin bath, a model-building platform, and ultraviolet laser for curing. To fabricate the desired model the layers are cured successively, and bonded together from bottom to top. As the first layer is polymerized the model-building platform is brought down inside the bath, and another layer of resin is added and cured. This process continues until the desired model is completed.

In 3D printing system the material is extruded from a nozzle that solidifies as soon as it is deposited on the manufacturing platform. The layer pattern is achieved through horizontal nozzle movement and interrupted material flow. This is followed by vertical movement for the sequential layer deposition.

The captured 3D data of model slice into cross-sections by a certain thickness. Inputting the processing parameters based on the contour information of each layer sheet allows for the automatic generation of the numerical code. Finally, a 3D object consisting of a series of layers is formed by stacking. This technology can receive CAD data directly and create new samples or models quickly without need for molds, cutting tools, or tooling fixtures.

Thanks to this technology, wasting less material, employing less human power, decreasing treatment time at the chair side, decreasing treatment cost, and lowering the rates of contamination, is possible.

In this study, a combination of conventional technique and RP will be used to fabricate complete dentures to overcome the polymerization shrinkage which results from conventional processing.

Explanation for choice of comparators:

Heat processed denture base is the treatment of choice for most of edentulous patients and it is considered as the golden standard and the main comparator for the new techniques. But using Heat Cured Acrylic resin would require many laboratory steps which introduce several errors.[14] Meanwhile, the introduction of rapid prototyping method with high accuracy which eliminates some of the laboratory steps was the reason for choosing it to compare it with the conventional method

Study Type

Interventional

Enrollment (Anticipated)

13

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

40 years to 70 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Cooperative patients with well developed ridges..

Exclusion Criteria:

  • Pathological changes of residual ridges.
  • Patients with any systemic diseases.
  • Patients with xerostomia.
  • Patients with flabby and flat ridges.
  • Patients with allergy to resins.
  • Patient with sever undercuts, or irregular bony exostosis.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Non-Randomized
  • Interventional Model: Crossover Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Placebo Comparator: conventional dentures
a complete denture made through conventional processing technique
conventional dentures
Active Comparator: 3D printed dentures
a complete denture made through 3d printing
construction of a 3d printed denture through a recent method instead of conventional heat processing

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Accuracy in terms of dimensional changes in denture base
Time Frame: immediately after denture construction
we will use radio-opaque markers to measure accuracy on software
immediately after denture construction

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Anticipated)

August 1, 2018

Primary Completion (Anticipated)

January 1, 2019

Study Completion (Anticipated)

April 1, 2019

Study Registration Dates

First Submitted

July 5, 2018

First Submitted That Met QC Criteria

August 2, 2018

First Posted (Actual)

August 3, 2018

Study Record Updates

Last Update Posted (Actual)

August 3, 2018

Last Update Submitted That Met QC Criteria

August 2, 2018

Last Verified

August 1, 2018

More Information

Terms related to this study

Other Study ID Numbers

  • hadeer's protocol

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Undecided

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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