Assessment of Customized 3D Zirconium Versus Titanium Mesh for Anterior Maxillary Ridge Augmentation With Delayed Implant Placement

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

ACTIVE_NOT_RECRUITING

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-09-01

Study Completion Date

2026-02-01

Brief Summary

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The aim of the present study is to assess the customized 3D zirconium versus titanium mesh for anterior maxillary ridge augmentation with delayed implant placement.

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Detailed Description

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Conditions

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Ridge Augmentaton and Dental Implants Bone Loss, Alveolar

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Group I (controlled group):

\- Ten sites of anterior maxillary ridge atrophy will be treated by titanium mesh with bone graft with delayed implant placement.

Group II (tested group):

\- Ten sites anterior maxillary ridge atrophy will be treated by zirconium mesh with bone graft with delayed implant placement.

Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Caregivers Outcome Assessors

Study Groups

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Group I (controlled group): -

Group I (controlled group):

\- Ten sites of anterior maxillary ridge atrophy will be treated by titanium mesh with bone graft with delayed implant placement.

Group Type OTHER

titanium mesh with bone graft with delayed implant placement.

Intervention Type DEVICE

titanium mesh with bone graft with delayed implant placement.

Group II (tested group):

Group II (tested group):

\- Ten sites anterior maxillary ridge atrophy will be treated by zirconium mesh with bone graft with delayed implant placement.

Group Type EXPERIMENTAL

zirconium mesh with bone graft with delayed implant placement.

Intervention Type DEVICE

zirconium mesh with bone graft with delayed implant placement.

Interventions

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titanium mesh with bone graft with delayed implant placement.

Intervention Type DEVICE

zirconium mesh with bone graft with delayed implant placement.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

1. Patients from both genders with the age range of 18-60 years with good systemic health, no contraindication for periodontal surgery and able to maintain good oral hygiene.
2. Patient with anterior maxillary alveolar ridge deficiency (horizontal, vertical or combined defects) less than 2 mm in width or less than 6 mm in height - measured from the alveolar crest to the basal bone in order to be enrolled in this study. (56)
3. Adequate zone of keratinized gingiva at minimum 3mms.
4. Patient with sufficient inter-arch space for future dental rehabilitation.
5. Subjects who are not on any medication known to interfere with periodontal tissue health or healing within 6 months of the study.

Exclusion Criteria

1. History of systemic diseases (i.e. diabetes, autoimmune dysfunction, prolonged cortisone therapy, or chemotherapy) that would contraindicate periodontal surgical treatment or affect bone turn over.
2. Patients with deleterious habits like the use of tobacco chewing or smoking ones.
3. History of previous periodontal surgical treatment of the involved sites.
4. Presence of malocclusion and pathologic movement of teeth in involved sites.
5. Patient not willing to give consent for the study and poor plaque control.(57)
6. Pregnant or nursing mothers.
7. Patients with acute odontogenic infection.

Minimum Eligible Age

20 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No