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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06450535
Other study ID # CEBD_CU_2024_26_1
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date July 1, 2024
Est. completion date December 1, 2025

Study information

Verified date June 2024
Source Cairo University
Contact maria ibrahim nageeb, BSc
Phone 01002402712
Email maria.nageeb@dentistry.cu.edu.eg
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Two groups of patient with horizontally deficient anterior maxilla indicated for bone augmentation ,one will be subjected to autogenous onlay bone block from retromolar bone and the other to cortical shell from retromolar bone also.


Description:

- Two groups of patients with horizontally deficient anterior maxilla indicated for bone augmentation, the first group will be subjected to autogenous onlay bone block from retromolar bone and the other group to cortical shell from retromolar bone also. - periodontal therapy will be performed before any procedure and oral hygiene measures will be given to the patient. - After injecting local anesthesia in the anterior maxillary region a trapezoidal flap will be performed in the area of horizontal bone defect (the recipient site). - The recipient site will be decorticated and recontoured using a round bone bur for better adaptation of the graft and to improve graft-to-recipient bone contact. - Bone harvesting will be carried out from retromolar region (the donor site) a crestal incision will be carried out 5 mm below and parallel to the gingival margin of the mandibular molars. - subperiosteal dissection will be extended to expose the ascending ramus and the retromolar region. - Using piezoelectric device a crestal cut and two proximal vertical cuts penetrating the cortex of the external oblique ridge will be performed then the inferior cut will be carried out. - Using a mallet and chisel the bone block will be sheared off. - The underlying cancellous bone will be gently retrieved and the collected bone will be conserved in sterile saline, followed by suturing the mucosal wound. - Onlay bone block graft procedure (control group) - In the first intervention, a bone block harvested from the donor site will be fixed with osteosynthesis titanium screws to the recipient site as an onlay graft to achieve a horizontal enlargement of the alveolar ridge. - Cortical shell graft procedure (intervention group) - The harvested cortical plate will be split longitudinally in two parts using a micro-saw and thinned with the bone scraper to achieve a plate of 1 mm thickness. - The plate will be fixed at a distance from the residual ridge with 2 screws. - Autogenous bone particles, collected with the bone scraper, were tightly packed into the gap between the plate and the recipient site. - Radiographic assessment will be achieved by CBCT scan immediately and 4 months postoperatively to evaluate bone regeneration and final horizontal bone width. - In the two groups, the screws will be removed 4 months postoperatively after final CBCT. - The bone formed in the gap between the bone segment and the original bone will be measured from the CBCT scan. - Before the intraoperative installment of the dental implants, bone core biopsies will be retrieved from each patient's recipient sites followed by implant placement.


Recruitment information / eligibility

Status Recruiting
Enrollment 16
Est. completion date December 1, 2025
Est. primary completion date December 1, 2025
Accepts healthy volunteers No
Gender All
Age group 20 Years to 60 Years
Eligibility Inclusion Criteria: - Patients in both sex with partial edentulism of the maxilla and requiring horizontal ridge augmentation - The ages of the patients ranged from 20 to 60 years. - The residual ridge width in these patients are less than 4.m - Sufficient bone in intra-oral donor sites are available (external oblique ridge) - Patients free from any systemic conditions and bone metabolism diseases that might interfere with the surgical intervention, soft tissue or hard tissue healing. - The vertical level should be in a favourable esthetic appearance with normal inter-arch space - The minimum number of missing teeth in the anterior maxilla alveolar ridge is one single extracted teeth Exclusion Criteria: - Subjected to irradiation in the head and neck area less than 1 year before implantation. - Poor oral hygiene and motivation. - Uncontrolled diabetes. - Pregnant or nursing. - Substance abuse. - Psychiatric problems or unrealistic expectations. - Severe bruxism or clenching. - Immunosuppressed or immunocompromised.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Autogenous onlay bone block harvesting from retromolar bone in anterior maxilla
Surgical protocol ( retromolar bone harvesting) After injecting local anesthesia a crestal incision is done, from a point on the occlusal surface along the external oblique ridge and extending anteriorly and inferiorly through the buccal mucosa, parallel to the gingival margin of the mandibular molars. The subperiosteal dissection extend to expose the ascending ramus and the retromolar region With the aid of surgical carbide burs, two proximal vertical cuts penetrating the cortex of the external oblique ridge. The depth of penetration of the posterior cut did not exceed 2.5 mm to avoid injury to the inferior alveolar nerve. By using microsaw , an inferior cut of 3.2 mm in depth joining the anterior and posterior vertical cuts was done. Small perforations of 3-4 mm in depth were performed on the superior aspect of the external oblique ridge using 1 mm drill bur. Finally, the block was sheared off using a chisel.
Autogenous cortical shell technique from retromolar bone in anterior maxilla
The harvested cortical plate was then split longitudinally in two parts using a microsaw, and thinned with the bone scraper to achieve a plate of 1 mm thickness. The plate was fixed at a distance from the residual ridge with 2 screws. Autogenous bone particles, collected with the bone scraper, were tightly packed into the gap between the plate and the recipient site.

Locations

Country Name City State
Egypt faculty of oral and dental medicine ,Cairo university Cairo Giza

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary radiographic analysis calculation of bone width gain using cone beam computed tomography 4 month postoperative
Secondary histomorphometric analysis to assess the bone quality for each technique 4 months postoperative
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