Retention, Chewing Efficiency and Masticatory Performance of Partial Dentures Opposing Implant Retained Prosthesis.

Implant Complication Clinical Trial

Official title:

Retention, Chewing Efficiency and Masticatory Performance of Maxillary Flexible Versus Computer Aided Design/Computer Aided Manufacture(CAD/CAM) Partial Dentures Opposing Fixed Implant Retained Prosthesis.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05999760
• Other study ID #: Elhotieby.M
• Status: Completed
• Phase: N/A
• Start date: November 15, 2022
• Est. completion date: January 20, 2023

Study information

• Verified date: August 2023
• Source: National Research Centre, Egypt
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study aims to evaluate retention ,chewing efficiency and masticatory performance of flexible versus CAD/CAM partial dentures opposing to fixed implant retained restorations.

Description:

in this study 22 patients will be selected following inclusion and exclusion criteria. The patients will be divided randomly into two groups.

Group I patients will receive Versacrylic removable partial denture. group II patients will receive CAD/CAM removable partial denture all patients will be given the home care instructions at night and brush cleaning of the dentures.

Measurements of retention using universal testing machine, masticatory performance using T-scan III computerized system and chewing efficiency using chewing function questionnaire

Recruitment information / eligibility

• Status: Completed
• Enrollment: 22
• Est. completion date: January 20, 2023
• Est. primary completion date: January 15, 2023
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 40 Years to 50 Years

Eligibility

Inclusion Criteria:

• Non-smoker male Patients

• Age ranging from 40-50 years.

• Highly cooperative and motivated patients.

• Patients Systemically free from any immunosuppressive diseases.

• Patients free from Diabetes, Hypertension, Cancer, any mental or physical diseases.

• Patients not receiving any Radiotherapy or chemotherapy treatment.

Exclusion Criteria:

• Female patients

• Smoker patients.

• Age exceeding 50 years

• Uncooperative and unmotivated patients.

Related Conditions & MeSH terms

• Implant Complication
• Implant Site Reaction

Intervention

Device:
• evaluation of retention of Versacryle and CAD/CAM partial dentures by force gauge
Evaluation of retention of Versacryle and CAD/CAM partial dentures by force gauge on day one, on first month, and on the second month of prosthesis delivery.
• chewing efficiency by electromyograph(E.M.G)
Evaluation of chewing efficiency of Versacryle and CAD/CAM partial dentures by force gauge on day one, on first month, and on the second month of prosthesis delivery.

Other:
• masticatory performance(questionnaire)
Evaluation of masticatory performance of Versacryle and CAD/CAM partial dentures by questionnaire on day one, on first month, and on the second month of prosthesis delivery.

Locations

Country	Name	City	State
Egypt	National Research Centre	Giza

Sponsors (1)

Lead Sponsor	Collaborator
National Research Centre, Egypt

Country where clinical trial is conducted

Egypt, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	evaluation of change of retention of versacrylic and CAD/CAM partial denture	measurement of retention of partial dentures made of Versacryle and CAD/CAM technology	on day 1 ,1 month and 2months of prosthesis delivery
Primary	evaluation of change of chewing efficiency of versacrylic and CAD/CAM partial denture	measurement of chewing efficiency of partial dentures made of Versacryle and CAD/CAM technology	on day 1 ,1 month and 2months of prosthesis delivery
Primary	evaluation of change of masticatory performance of versacrylic and CAD/CAM partial denture	measurement of masticatory performance of partial dentures made of Versacryle and CAD/CAM technology	on day 1,1 month and 2months of prosthesis delivery