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

NCT ID: NCT06109519

Last Updated: 2023-10-31

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

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-02-16

Study Completion Date

2023-09-16

Brief Summary

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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

Detailed Description

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Conditions

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Prosthesis User

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

All patients in this study will be divided into two equal groups Group I (control): patients who would be delivered mandibular implant overdenture using conventional locator attachments.

Group II (study): patients who would be delivered mandibular implant overdenture using Locator RTX attachments
Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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Group I

patients who would be delivered a mandibular implant overdenture using conventional locator attachments.

Group Type ACTIVE_COMPARATOR

implant supported overdenture

Intervention Type PROCEDURE

patients would be delivered mandibular implant overdenture using conventional locator and Locator RTX attachments

Group II (study)

patients who would be delivered mandibular implant overdenture using Locator RTX attachments

Group Type ACTIVE_COMPARATOR

implant supported overdenture

Intervention Type PROCEDURE

patients would be delivered mandibular implant overdenture using conventional locator and Locator RTX attachments

Interventions

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implant supported overdenture

patients would be delivered mandibular implant overdenture using conventional locator and Locator RTX attachments

Intervention Type PROCEDURE

Eligibility Criteria

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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
Minimum Eligible Age

45 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Mansoura University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Mansoura University ,Faculty of dentistry

Al Mansurah, , Egypt

Site Status

Countries

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Egypt

Other Identifiers

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A0208023RP

Identifier Type: -

Identifier Source: org_study_id