Comparison of Flexural Strength and Flexural Modulus of Conventional and Graphene-Reinforced Polymethyl Methacrylate

November 18, 2025 updated by: Wajiha Zia, Altamash Institute of Dental Medicine

Study Title: Comparison of Flexural Strength and Modulus of Conventional and Graphene-Reinforced PMMA

Introduction:

This in-vitro experimental study aims to compare the flexural strength and flexural modulus of conventional polymethyl methacrylate (PMMA) and graphene-reinforced PMMA (G-PMMA) used in denture bases. PMMA is widely used for dentures due to its affordability, aesthetics, and biocompatibility but has limitations such as low flexural strength and susceptibility to fracture. Graphene, a strong and flexible nanomaterial, has demonstrated potential in enhancing PMMA's mechanical properties.

OBJECTIVE:

To compare the flexural strength and flexural modulus of conventional and graphene reinforced polymethyl methacrylate

HYPOTHESIS:

Null Hypothesis:

There is no difference in flexural strength and flexural modulus of graphene reinforced PMMA and conventional PMMA.

Alternative Hypothesis:

There is a difference in flexural strength and flexural modulus of graphene-reinforced PMMA and conventional PMMA.

Methodology:

  • Study Design: In-vitro experimental trial
  • Study SETTING:

    • The study will be carried out at Altamash Institute of Dental Medicine in the department of prosthodontic, Karachi Pakistan.
    • The graphene (Miraculum Graphene Private Limited,Gujrat, Ahmedabad,India) will be reduced at Karachi University's Food Science Department.
    • For the formation of mold, the digital metal bar (CoCr, Eplus3D, Hangzhou China) will be fabricated by Selective laser melting (SLM) (Audental Shanghai, East-central China) at Chughtai Lab in Peshawar, Pakistan.
    • The acrylic (Mr. Teeth, Royale Elite, Surrey,United Kingdom) samples will be cured by short curing cycling in the prosthodontic department at Bahria dental University, Karachi.
    • The thermocycling (thermocycler, San Francisco, USA) and universal testing for flexural strength and modulus of acrylic samples will be performed at the research laboratory of Dow University of health sciences.
  • Sample Size: The projected sample size for this study is 76 specimen, 38 samples per group by comparing two means in open epi software19 (version 3).The calculation was based on the result of Kaan Yerliyurt 11 study, considering the mean value of 68.16 MPa and standard deviation (SD) of 5.79 MPa for the experimental group and the mean value of 72.6 MPa and standard deviation (SD) of 7.84 MPa for the control group of flexural strength. The analysis accounts for multiple time intervals, and the significance level (α) is set at 0.05, with a power of 80%, confidence interval (CI) of 95%, a margin of error (ME) of 5%.

    76 specimens (38 for conventional PMMA, 38 for G-PMMA)

  • Subgroups: Each group will have thermocycled and non-thermocycled samples to assess durability.

SAMPLING TECHNIQUE:

Stratified sampling followed by systematic division.

  • Methodology:
  • Thermocycling: 2000 cycles (5°C-55°C) simulating oral temperature variations

Data Collection:

A metal bar mold (65 mm × 10 mm × 3 mm) will be designed using Exocad CAD software and 3D-printed from CoCr material using Selective Laser Melting (SLM). After fabrication, the bar will be used to create a silicone mold, which will then be invested in dental plaster to prepare the final mold for specimen curing. Graphene oxide (GO) will be chemically reduced, purified, dried, and mixed into PMMA powder. The acrylic resin will then be packed into the mold and processed via short curing cycle (74°C for 2 hours, 100°C for 1 hour). Then all the specimen will be prepared, thermocycle and ready for flexural strength and flexural modulus.

- Data Analysis: The data will be evaluated using the statistical package for social sciences (SPSS version 29, IBM, Chicago, Illinois United States). Descriptive statistics will be evaluated by mean, standard deviation, median, interquartile range of flexural strength, flexural modulus for PMMA, and GPMMA. Shapiro-Wilk test will be used to check the normality of the data distribution. For interferential statistics, Kruskal Wallis or ANOVA will be used with factors of loading force (N) and deflection (Y) between G-PMMA and conventional PMMA. Post-hoc analysis will be performed by Bonferroni or Tukey's test. In order to assess the effect of the external environment, the cofounding variable in this study will be thermocycling, which will influence the flexural strength and flexural modulus of PMMA and graphene-reinforced PMMA samples. A Chi-square or independent t-test will be used to analyze the impact of the cofounding variable, thermocycling, on flexural strength and modulus. The level of significance will be set at p < 0.05.

Rationale:

This study aims to determine whether graphene reinforcement improves the mechanical properties of PMMA, potentially leading to stronger and more fracture-resistant dentures. The findings could contribute to the development of more durable denture base materials with enhanced longevity and performance.

Study Overview

Status

Active, not recruiting

Intervention / Treatment

Study Type

Interventional

Enrollment (Estimated)

76

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

      • Karachi, Pakistan
        • Altamash institute of dental medicine
    • Sindh
      • Karachi, Sindh, Pakistan
        • Altamash institute of dental medicine

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

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • INCLUSION CRITERIA:

    • Samples that are dimensionally accurate in accordance to ISO Standard 178.21
    • Sample that are free from surface porosities like gaseous, granular or contraction porosities.
    • Samples have uniform color and surface texture indicating proper curing.
    • Samples free from crazing defects and warpage.
    • Samples with no signs of distortion after thermocycling.
    • Samples with homogeneously distributed graphene by visual inspection of samples.

Exclusion Criteria:

  • • Samples with incorrect mixing ratio of base to catalyst.

    • Samples in which the metal bar is partially exposed.
    • Samples that are not fully embedded in plaster.
    • Samples showing sign of contamination from foreign body during packing process.
    • Samples with improper mixing of plaster shows a sign of cracks and voids surrounding the samples.
    • Samples in which the flask will not properly sealed during flasking.
    • Samples fractured due to thermocycling.
    • Samples fractured during handling or transportation before testing.

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

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: PMMA(polymethyl methacrylate)
Polymethyl methacrylate (PMMA), which was invented by Dr. Walter Wright1 in 1937, and is now one of the most widely used denture base materials. Polymethyl methacrylate (PMMA) has gained popularity due to its low cost, adequate mechanical strength, acceptable aesthetics, good dimensional stability, and biocompatibility. However, it has low flexural strength, fatigue fracture, and impact strength which can lead to fracture of the prosthesis.
Experimental: G-PMMA( Graphene-polymethyl methacrylate)
Graphene was first invented by Novoselov et al,16 Graphene is a two dimensional (2D), monolayer sp2 hybridized carbon atoms and recognized as the thinnest material in the universe. Comparing it to other traditional nanofillers, its large surface area, tensile strength, flexibility, strong thermal and electrical conductivity, and low coefficient of thermal expansion give it a better result.17 Recent studies have discovered that graphene and its derivatives, which include graphene oxide and reduced graphene oxide, have better outcomes as compared to conventional materials
The study follows an in-vitro experimental design with 76 specimens divided into two groups (conventional PMMA and G-PMMA). These samples will be further divided into two group, the one which undergo thermocycling (simulating oral temperature changes) and the other which don't undergo thermocycling. Flexural strength and modulus will be tested on all these by using a three-point bending test.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Flexural strength and Flexural modulus
Time Frame: 1 year

Outcome Measure 1: Flexural Strength (MPa) The flexural strength of the specimens will be measured using a three-point bending test on a universal testing machine (Testometric testing machine, model VB50-300, Rochdale, Greater Manchester, United Kingdom).

A load of 0N at a crosshead speed of 2 mm/min will be applied. The force will be increased until the specimens fracture. The maximum force (N) applied before fracture will be recorded to calculate the flexural strength (MPa).

Outcome Measure 2: Flexural Modulus (MPa) The flexural modulus of the specimens will be tested using a universal testing machine (Testometric testing machine, model VB50-300, Rochdale, Greater Manchester, United Kingdom).

A constant load of 0N at a crosshead speed of 2 mm/min will be applied. The load (N) and deflection (Y) will be recorded using WinTest software. The initial slope of the load-deflection curve (elastic region) will be used to determine flexural modulus (MPa).

1 year

Collaborators and Investigators

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

Investigators

  • Study Director: Dr.Naseer Ahmed, Bds,Fcps,PhD, Altamash institute of dental medicine

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)

February 24, 2025

Primary Completion (Estimated)

December 25, 2025

Study Completion (Estimated)

January 25, 2026

Study Registration Dates

First Submitted

February 10, 2025

First Submitted That Met QC Criteria

February 28, 2025

First Posted (Actual)

March 4, 2025

Study Record Updates

Last Update Posted (Actual)

November 19, 2025

Last Update Submitted That Met QC Criteria

November 18, 2025

Last Verified

November 1, 2025

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • AltamashWZ

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

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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