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NCT06080815 Clinical Trial

Impact of Mandibular Overdenture Base Construction Techniques on Assessment of Occlusion

Prosthesis Durability Clinical Trial

Official title:
Impact of Mandibular 4-Implant Overdenture Base Construction Techniques on Assessment of Occlusion With Digital Occlusion Analysis System (Within Patient Study)

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT06080815
Other study ID # 05201021
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 10, 2022
Est. completion date March 7, 2023

Study information
Verified date September 2023
Source Mansoura University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This within patient study will be conducted to compare between two different construction techniques (CAD-CAM Milled and Conventional techniques) of 4-implant-assisted complete mandibular overdenture bases regarding the digital occlusion force balance analysis using the OccluSense

Recruitment information / eligibility
Status Completed
Enrollment 30
Est. completion date March 7, 2023
Est. primary completion date December 15, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 40 Years to 70 Years
Eligibility Inclusion Criteria: - 1. Free from any systemic diseases that contraindicate dental implantation. 2. Angel's class I maxillo- mandibular relation. 3. Available inter-arch space and sufficient restorative space. 4. Nonsmokers, non-alcoholics. 5. Complaints from their conventional denture Exclusion Criteria: - diabetic and heavy smoker patients

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• CAD/CAM Complete denture
four implant-supported CAD/CAM complete overdenture

Locations
Country Name City State
Egypt Mansoura University Mansoura

Sponsors (1)
Lead Sponsor Collaborator
Mansoura University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary digital occlusal analysis occlusion was analyzed by occlusense device 6 months
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