Measurement of the Biting Force of Rabid Heat Cured Acrylic Resin Versus Modified Conventional Acrylic

NCT ID: NCT03006757

Last Updated: 2016-12-30

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

2 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-05-31

Study Completion Date

2017-12-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The purpose of this study is to compare the effect of rapid heat cured acrylic resin material with titanium dioxide nanoparticles added to conventional acrylic resin material on the biting force of the single maxillary complete denture .

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Bite force is one indicator of the functional state of the masticatory system that results from the action of jaw elevator muscles modified by the craniomandibular biomechanics .Determination of individual bite force level has been widely used in dentistry, mainly to understand the mechanics of mastication for evaluation of the therapeutic effects of prosthetic devices and to provide reference values for studies on the biomechanics of prosthetic devices. In addition, bite force has been considered important in the diagnosis of the disturbances of the stomatognathic system .

Twenty (20) single maxillary completely edentulous patients were selected from the out-patient clinic of the Removable Prosthodontics Department, Faculty of Oral and Dental Medicine, Cairo University.

The primary outcome is to measure the biting force of single maxillary complete denture by I Load star sensor .

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Dental Anxiety

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

SINGLE

Investigators

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Column titanium dioxide

patient take titanium dioxide denture participants 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.

Group Type EXPERIMENTAL

titanium dioxide denture base

Intervention Type OTHER

column placebo

patient will take denture with conventional acrylic ( 20 minutes cure ) for 1 month in the initial phase

Group Type EXPERIMENTAL

titanium dioxide denture base

Intervention Type OTHER

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

titanium dioxide denture base

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* completely edentulous maxillary arch and full or partial dentate mandibular arch with adequate inter arch space
* edentuluos arches should be covered by firm healthy mucosa angle class 1 maxillomandibular relationship

Exclusion Criteria

* patients with bad habits
* previous history of radiotherapy or chemotherapy
Minimum Eligible Age

30 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

emad gamal ismail

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

emad gamal ismail

principal invistigator

Responsibility Role SPONSOR_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Mahmoud Adly

Giza, Giza Governorate, Egypt

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

Egypt

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

mahmoud adly radwan, master

Role: CONTACT

Phone: 00201009714746

Email: [email protected]

mahmoud adly radwan, bachelor

Role: CONTACT

Phone: 00201009714746

Email: [email protected]

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

mahmoudd 002 radwan, bachelor

Role: primary

emad 002 gamal, bachelor

Role: backup

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

900

Identifier Type: -

Identifier Source: org_study_id