- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06856239
Comparison of Flexural Strength and Flexural Modulus of Conventional and Graphene-Reinforced Polymethyl Methacrylate
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
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Karachi, Pakistan
- Altamash institute of dental medicine
-
-
Sindh
-
Karachi, Sindh, Pakistan
- Altamash institute of dental medicine
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
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
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
Investigators
- Study Director: Dr.Naseer Ahmed, Bds,Fcps,PhD, Altamash institute of dental medicine
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
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)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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