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Clinical Trials/NCT05198011
NCT05198011CompletedNot Applicable

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

Hams Hamed Abdelrahman1 site in 1 country14 target enrollmentStarted: October 1, 2019Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
14
Locations
1
Primary Endpoint
Operation time

Study 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
40 Years to 60 Years (Adult)
Sex
All
Accepts Healthy Volunteers
No

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

Arms & Interventions

3D mandibular ridge augmentation

Experimental

Intervention: 3D customized Titanium Mesh (Study) (Procedure)

Conventional mandibular ridge augmentation

Active Comparator

Intervention: Conventional ridge augmentation (Control) (Procedure)

Outcomes

Primary Outcomes

Operation time

Time Frame: During the procedure

Time of operation for each group will be calculated

Change in bone volume

Time Frame: at baseline and 6 months

Bone volume wa measured using CBCT

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Hams Hamed Abdelrahman
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Hams Hamed Abdelrahman

Assistant lecturer of DPH and Clinical statistician

Alexandria University

Study Sites (1)

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