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Smart Box With OT Equator Attachment in Retaining Implant-assisted Overdenture for the Atrophic Maxilla.

NCT ID: NCT05352620

Last Updated: 2022-04-29

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

10 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-03-01

Study Completion Date

2019-05-01

Brief Summary

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The aim of the present study is to clinically and radiographically evaluate the effect of the use of recently developed Smart Box accompanied with OT Equator attachment in retaining of the inclined implant assisted overdenture for atrophic maxilla and to compare the vertical bone changes around axial implants with OT Equator attachment and inclined implants with smart box attachment radiographically using CBCT

Detailed Description

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Conditions

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Atrophic Maxilla Edentulous Jaw

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Implant assisted maxillary overdenture

Horseshoe Maxillary Complete overdenture construction (Stabilizing and connecting the Smart Box housing)

Group Type EXPERIMENTAL

Implant assisted maxillary overdenture

Intervention Type OTHER

For each patient, an implant assisted maxillary overdenture will be fabricated using a minimally invasive flapless surgical technique with OT-Equator and Smart Box attachment

Interventions

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Implant assisted maxillary overdenture

For each patient, an implant assisted maxillary overdenture will be fabricated using a minimally invasive flapless surgical technique with OT-Equator and Smart Box attachment

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Male patients with comparable age (30- 65 years).
* All patients should have retruded, posteriorly atrophic completely edentulous maxilla with sinus pneumatization leaving less than 7mm bone height posteriorly and a sufficient amount of bone in the inter bicuspids region.
* Opposing mandibular dentate arch including bilateral posterior teeth.
* All patients should have an adequate zone of keratinized mucosa.
* All patients should be free from any intra-oral or systemic diseases that would otherwise affect the osseointegration of dental implants.
* All patients should be well motivated, cooperative, and with adequate manual dexterity necessary to place and remove removable implant prosthesis to provide adequate oral hygiene around the endosseous implants.

Exclusion Criteria

* Patients with flabby maxillary ridges.
* Patients who are unwilling to accept implant overdentures as a treatment modality.
* Patients with temporomandibular and neuromuscular disorders.
Minimum Eligible Age

30 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Hams Hamed Abdelrahman

OTHER

Sponsor Role lead

Responsible Party

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Hams Hamed Abdelrahman

Assistant lecturer of DPH and Clinical statistician

Responsibility Role SPONSOR_INVESTIGATOR

Locations

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Alexandria Faculty of Dentistry

Alexandria, , Egypt

Site Status

Countries

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Egypt

Other Identifiers

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Overdenture_2022

Identifier Type: -

Identifier Source: org_study_id