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Microbiological Study on Maxillary Complete Dentures of Two Different Materials

Not Applicable
Conditions
Denture Stomatitis
Interventions
Other: titanium dioxide denture
Other: rapid heat denture
Registration Number
NCT02950623
Lead Sponsor
Cairo University
Brief Summary

Cross over design the investigator divide participants to two groups group (A) will receive rapid heat cured denture base material and group (b) will receive the acrylic denture modified by titanium dioxide nanoparticles and after washout period alternatively group (a) will receive the acrylic denture modified by titanium dioxide nanoparticles AND group (b) will receive rapid heat cured denture base material the investigator will take swaps from dentures to count the anaerobic bacteria.

Detailed Description

First the investigator will take primary impression, and pour it obtain primary cast, then will fabricate special tray an take secondary impression and obtain master cast after that duplication of master cast will be done the investigator will make cross over design.and divide participants to two groups group (A) will receive rapid heat cured denture base material and group (b) will receive the acrylic denture modified by titanium dioxide nanoparticle and after washout period alternatively group (a) will receive the acrylic denture modified by titanium dioxide nanoparticle AND group (b) will receive rapid heat cured denture base material the investigator will take swaps from the different dentures to count the anaerobic bacteria by (CFU).

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
2
Inclusion Criteria
  1. Completely edentulous maxillary arch and partially dentate mandibular arch with adequate interarch space.
  2. The edentulous ridges should be covered by firm healthy mucosa. 3-Angle class I maxillomandibular relation. 4-Healthy and cooperative patient
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Exclusion Criteria
  1. Patients with bad habits as severe clenching or bruxism, drug or alcohol addiction, moderate or heavy smoking (greater than 10 cigarettes per day).
  2. Previous history of radiotherapy or chemotherapy.
  3. Any skeletal problem dictates surgical intervention
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Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
patients take rapid heat denturerapid heat denturepatients will receive rapid heat denture for 1 month in the initial phase of the trial then in the later phase patients will receive titanium dioxide denture (made from conventional acrylic resin modified by titanium dioxide nanoparticles )
patients take rapid heat denturetitanium dioxide denturepatients will receive rapid heat denture for 1 month in the initial phase of the trial then in the later phase patients will receive titanium dioxide denture (made from conventional acrylic resin modified by titanium dioxide nanoparticles )
patients take titanium dioxide denturerapid heat denturepatients will receive titanium dioxide denture (made from conventional acrylic resin modified by titanium dioxide nanoparticles ) for 1 month in the initial phase of the trial then in the later phase after one month they will receive( rapid heat cured acrylic resin)denture
patients take titanium dioxide denturetitanium dioxide denturepatients will receive titanium dioxide denture (made from conventional acrylic resin modified by titanium dioxide nanoparticles ) for 1 month in the initial phase of the trial then in the later phase after one month they will receive( rapid heat cured acrylic resin)denture
Primary Outcome Measures
NameTimeMethod
Microbiological investigation: Count of anaerobic bacteria on the fitting surface of denture by (CFU) unit6 months

Microbiological investigation: Count of anaerobic bacteria on the fitting surface of denture by (CFU) unit

Secondary Outcome Measures
NameTimeMethod
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