Three Dimensional Printed Versus Conventional Heat Cured Acrylic Complete Denture

November 6, 2022 updated by: Suez Canal University

Three Dimensional Printed Versus Conventional Heat Cured Acrylic Complete Denture: An In-Vivo Comparative Study

Introduction:

One major complaint frequently voiced by complete denture wearers is denture retention. Conventional denture disadvantage is heat-curing resin deformation. In addition, the pack and press technique that is still more common, residual stresses that occur at the time of packing are released when the material is removed from the flask, causing the resin to shrink, and this shrinkage is cited as a cause of poor fit of the denture base, In the field of prosthetic dentistry, the ability of additive manufacturing to fabricate prosthetic devices based on CAD data influences the overall quality, the mechanical properties of printed parts, the total cost and the manufacturing time. The milling process wastes large quantities of denture base material, and more recent three-dimensional (3D) prototyping promises a more sustainable additive approach by using less denture resin. However, no clinical reports have been published regarding the accuracy of the mucosal surface or denture retention for denture fabricated using conventional techniques compared to those fabricated using additive manufacturing.

Aim of the study:

Investigate the effect of two techniques of complete denture manufacturing (conventional and 3D printed) on denture retention, trueness (accuracy), and satisfaction.

Methodology:

Twenty patients will be selected from the outpatient clinic and will be divided into 2 groups, group A for conventional dentures and group B for 3D printed dentures, retention for the two groups will be measured at 0,1 and 3 months, and patient satisfaction will be recorded, and accuracy of the denture base will be measured on the software. The results will be tabulated and statistically analyzed using the SPSS program.

Study Overview

Detailed Description

Twenty patients will be selected from the Faculty of Dentistry (Suez Canal University) outpatient clinics with the following criteria:

  • Patients with good neuromuscular control and free of systemic diseases
  • Well-formed ridges with firm and healthy mucosa and no bilateral anterior undercuts.

The patients will be divided equally into two groups(n=10), group (A) which will receive conventional heat cure acrylic denture, and group (B) which will receive 3D printed denture.

Methodology:

A primary impression will be taken for each patient and a special self-cured acrylic tray will be fabricated.

Zinc oxide secondary impression (caves outline, Cavex Holland)will be taken for each patient. The impression will be poured with extra hard stone and labeled master cast.

The cast will be scanned and saved in standard tessellation language (stl) format (master cats).

Jaw relation records for each patient will be taken in the conventional method. For group A: the setting up of teeth will be done in a conventional way on the articulator, and flasking of the waxed-up denture will be done. Wax elimination will be done then packing of heat cure acrylic will be done.

For group B: occlusion block will be scanned (swing scanner, DOF inc, Korea)(the scanner has an accuracy of 10 μm) after taking jaw relation record.

Virtual teeth form, size, and setting will be done on the CAD software (Exocad Dental CAD 3.0, Exocad GmbH, Germany) according to jaw relation record.

The denture base extension and thickness will be designed on CAD software. The teeth will be exported in a separate file and the denture base will be exported in a separate stl file.

The virtual denture stl files will be sent to the 3D printer software (Chitubox software, CBD-Tech, china) where slicing of the file and adjustment of layers setting will be done.

The virtual denture will be sent to the 3D printer (photon 3d printer, ANYCUBIC 3D Printing, china) to be printed (printer has Y axis resolution: 1.25um and Layer resolution: 25 ~ 100um), Teeth will be printed alone using tooth-colored resin(dental sand, Harz labs, Russia) and base will be printed alone using pink resin(dental pink, HArzz lab, Russia), then it will be ethyl alcohol washed (99% ethyl alcohol) to remove excess resin. The teeth will be placed in their places in the denture base and secured using pink resin.

Post-curing for remaining uncured resin will be done using a post-curing chamber for 30 minutes (bre-lux power unit 2,bredent, united kingdom).

Regarding the maxillary denture:

Retention will be measured clinically by using a force gauge (weihang electronic gauge,weihang industries, china) for group A and group B at 0,1 and 3 months. A force gauge will be applied by fixing the chain at the center of the polished surface of the denture. The pull end of the force gauge will be connected to the denture to measure the retention. The force gauge will pull the denture vertically downward until denture retention will be lost, and the denture will move vertically. The force at which the denture dislodges will be recorded in grams. The pull-off procedure will be repeated 10 times to obtain 10 records for each elder, and then the mean of these records will be calculated.

Participants will answer a denture satisfaction questionnaire. Possible answers for each question and respective scores will be: unsatisfactory =0, regular =1, and good =2 (Rehmann et al., 2008) For group, A and group B denture base will be checked for accuracy of fit after scanning using a bench scanner with 1.3 megapixels dual camera and 10-micron accuracy (swing scanner, DOF inc, Korea) and will be compared to the virtual one planned on the master cast using metrology software (Geomagic Control X,3D systems, Canada). This will be done by the superimposition of the scanned printed or processed denture and the virtual reference denture. This will be done by selecting a point-to-point match and then the best fit function.

Color maps of the surface matching differences will be done. Areas that will be yellow to red in color will indicate impingement of the denture base with the cast. Areas that will be blue in color will indicate space between the denture base and cast. The ideal denture will show a color map that will be entirely green, giving a measurement value of 0, which will represent no processing deformation and an ideal adaptation of the denture base to the cast.

The results will be tabulated and statistically analyzed using SPSS Statistics Version 20 for Windows (SPSS, Inc., an IBM Company, USA).

Study Type

Interventional

Enrollment (Actual)

20

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 Locations

    • Sharkia
      • Bilbeis, Sharkia, Egypt, 46213
        • Faculty of Dentistry,Suez Canal University

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

50 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Patients with good neuromuscular control and free of systemic diseases
  • the edentulous ridge was covered with healthy firm and dense mucosa
  • They have upper and lower edentulous healthy alveolar ridges with no remaining roots, no severe bony undercut, or local pathological lesions.
  • patients had no previous dentures with a nearly equal edentulous period.

Exclusion Criteria:

  • history of bad habits e.g. severe clenching.
  • T.M.J disorders
  • patients with xerostomia, high palatal vault, and short or hyperactive lips were excluded.

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: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: group A
group A will receive a conventional heat-cure acrylic denture
retention for the two groups will be measured at 0,1 and 3months, patient satisfaction will be recorded, and accuracy of the denture base will be measured on the software.
Active Comparator: group B
group B will receive a 3D printed complete denture
retention for the two groups will be measured at 0,1 and 3months, patient satisfaction will be recorded, and accuracy of the denture base will be measured on the software.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
accuracy of fit (adaptation)
Time Frame: 1 week
the deviation of the denture fiitng surface from its corresponding cast will be measured using metrology software (GOM inspect,USA))
1 week
retention
Time Frame: 3 months
retention will be measured using digital force gauge(weihang electronic gauge,weihang industries, china)
3 months
patient satisfaction
Time Frame: 3 months
Participants will answer a denture satisfaction questionnaire. Possible answers for each question and respective scores will be: unsatisfactory =0, regular =1, and good =2 (Rehmann et al., 2008)
3 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
retention over time period
Time Frame: 3 months
change in denture retention over time period(0,1 and 3 months from denture insertion) will be measured for each group
3 months

Collaborators and Investigators

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

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the 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 (Actual)

August 1, 2021

Primary Completion (Actual)

May 1, 2022

Study Completion (Actual)

August 1, 2022

Study Registration Dates

First Submitted

October 12, 2022

First Submitted That Met QC Criteria

October 14, 2022

First Posted (Actual)

October 18, 2022

Study Record Updates

Last Update Posted (Actual)

November 8, 2022

Last Update Submitted That Met QC Criteria

November 6, 2022

Last Verified

November 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • 318/2021

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Yes

IPD Sharing Supporting Information Type

  • Study Protocol

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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