Skip to main content
Clinical Trials/NCT05198011
NCT05198011
Completed
Not Applicable

Mandibular Ridge Augmentation Using Three-Dimensional Printed Model for Customization of Titanium Mesh

Hams Hamed Abdelrahman1 site in 1 country14 target enrollmentOctober 1, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Alveolar Bone Loss
Sponsor
Hams Hamed Abdelrahman
Enrollment
14
Locations
1
Primary Endpoint
Change in bone volume
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

Completely or partially edentulous patients suffer from resorption of the alveolar bone, they always seek rehabilitation which becomes challenging. Alveolar ridge augmentation is widely done now to offer these patients functional and esthetic restoration. Many techniques have been proposed to obtain good results of ridge augmentation. Titanium Mesh (TiMe) is widely used, also digital and computer-guided surgery now plays an important role to improve the techniques and results in ridge augmentation procedures.

Registry
clinicaltrials.gov
Start Date
October 1, 2019
End Date
April 30, 2020
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Hams Hamed Abdelrahman
Responsible Party
Sponsor Investigator
Principal Investigator

Hams Hamed Abdelrahman

Assistant lecturer of DPH and Clinical statistician

Alexandria University

Eligibility Criteria

Inclusion Criteria

  • Patients will have a posterior mandibular atrophic ridge
  • Distance between the crest of the ridge and the superior border of the inferior alveolar canal will be from 5 mm to 7 m
  • Adequate inter-arch space

Exclusion Criteria

  • Patients who have any uncontrolled systemic disease contraindicated to oral surgery ( Diabetes, hypertension, and patients under chemotherapy treatment )
  • Patients who have any relevant bone disease.
  • Patients who are smokers

Outcomes

Primary Outcomes

Change in bone volume

Time Frame: at baseline and 6 months

Bone volume wa measured using CBCT

Operation time

Time Frame: During the procedure

Time of operation for each group will be calculated

Study Sites (1)

Loading locations...

Similar Trials