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
• Status: Completed
• Phase: N/A
• 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
• 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

Related Conditions & MeSH terms

• Prosthesis User

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