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NCT05317039 Clinical Trial

Piezosurgical Buccal Plate Repositioning Technique for Horizontal Alveolar Ridge Augmentation

Alveolar Bone Loss Clinical Trial

Official title:
Evaluation of Piezosurgical Buccal Plate Repositioning Technique for Horizontal Alveolar Ridge Augmentation Comparing Between Two Different Grafting Materials (a Randomized Clinical Trial)

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT05317039
Other study ID # Piezosurgery_2021
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date August 15, 2021
Est. completion date June 30, 2022

Study information
Verified date March 2022
Source Alexandria University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Achieving prosthetically driven implant placement is a highly predictable treatment modality with reliable long-term results. Different surgical procedures have been used as a solution for reconstructing of the alveolar ridge with deficient volume. In the present study we demonstrate a modified alveolar ridge split technique for horizontal alveolar ridge augmentation (buccal plate repositioning technique) using the piezotome surgery. Evaluation of the effect of silica-calcium phosphate nanocomposite (SCPC) graft material versus demineralized freeze dried bone allograft (DFBA) in horizontal alveolar ridge augmentation before implant insertion will be performed.

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 18
Est. completion date June 30, 2022
Est. primary completion date June 30, 2022
Accepts healthy volunteers No
Gender All
Age group 20 Years to 50 Years
Eligibility Inclusion Criteria: - Patients with horizontal atrophy of the posterior mandible with pristine residual alveolar crest width from 2 to 4 mm. - Augmented area length in the mesial-distal direction of less than 20 mm. - Adequate physically healthy condition. Exclusion Criteria: - A systemic disease that would contraindicate oral surgical treatment. - Treated patients who had undergone therapy involving radiation - Patients who had received bone resection as part of an oncological treatment after a bone augmentation procedure. - Patients are subjected to intravenous and/or oral bisphosphonate therapy after the bone augmentation procedure.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• silica-calcium phosphate nanocomposite SCPC
Patients will be treated with the buccal plate repositioning technique and grafted with SCPC then the grafted defect will be covered with a platelet-rich fibrin membrane.
• freezed dried bone
Patients will be treated with the buccal plate repositioning technique and grafted using DFDBA. then the grafted defect will be covered with a platelet-rich fibrin membrane.

Locations
Country Name City State
Egypt Alexandria Faculty of Dentistry Alexandria

Sponsors (1)
Lead Sponsor Collaborator
Hams Hamed Abdelrahman

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary change in alveolar ridge width All patients will receive a CBCT scan; immediately after surgery and at 6 months post-operatively. The images will be analyzed using OnDemand3D software (Cybermed Inc) CBCT analyzing software and compared to the pre-operative scan for alveolar ridge width evaluation. at baseline and 6 months
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