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NCT06109519 Clinical Trial

Comparative Clinical Study for Two Types of Locator Attachments for Mandibular Implant Supported Overdenture

Prosthesis User Clinical Trial

Official title:
A Comparative Clinical Study for Two Types of Locator Attachments for Mandibular Implant-supported Overdenture; A 3-year Radiographic and Clinical Follow-up Study

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT06109519
Other study ID # A0208023RP
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 16, 2020
Est. completion date September 16, 2023

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

Clinical Trial Summary

This study aims to evaluate the clinical and radiographic outcomes for mandibular implant-supported overdenture using two different types of locator attachment after 3 years of using the two types of locator attachments

Recruitment information / eligibility
Status Completed
Enrollment 30
Est. completion date September 16, 2023
Est. primary completion date June 7, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 45 Years to 70 Years
Eligibility Inclusion Criteria: - 1. All selected patients have two implants placed in the mandibular interforaminal region. 2. All selected patients have a healthy mucosa and with no clinical complications. 3. All patients are cooperative and approve the proposed treatment protocol Exclusion Criteria: - 1. Patients who reject to participate in the study. 2.Patients who need implant placement as a result of previous implant failure

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• implant supported overdenture
patients would be delivered mandibular implant overdenture using conventional locator and Locator RTX attachments

Locations
Country Name City State
Egypt Mansoura University ,Faculty of dentistry Mansoura

Sponsors (1)
Lead Sponsor Collaborator
Mansoura University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary crestal cone loss Intraoral radiographs were performed using the long cone paralleling technique to evaluate crestal bone loss three years
Primary prosthetic complications prosthetic complications were scored clinically three years
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