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Evaluation of Horizontal Anterior Mandibular Augmentation With Split Bone Block Technique From the Chin

Evaluation of Horizontal Anterior Mandibular Augmentation With Split Bone Block Technique From the Chin

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06727591
Enrollment
10
Registered
2024-12-11
Start date
2023-10-10
Completion date
2024-10-20
Last updated
2024-12-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alveolar Bone Grafting

Brief summary

The aim of this study was to compare clinically and radiographically bone gain, healing of the surgical site, healing of the grafted bone and stability of the grafted area following horizontal ridge augmentation at anterior mandible using split bone block from the chin area.

Interventions

An intraoral crestal incision with/out vertical arms was performed on alveolar ridge using blade no.15. After flap reflection, patroning the defect to help guide the area to be grafted from the donor site. At the chin area (donor site) unicortical cuts will be made at least 5 mm inferior to root tips, 5 mm superior to inferior border of mandible and 5 mm away from the mental foramen. The graft was luxated and split into two bone shells each 1 \ 2 mm in thickness using disc. The bone shells and the donor site were scrapped for autogenous graft particles. Decortication of the recipient site. The graft was stabilised into the recipient site using two or more self tapping titanium screws placed midway corono-apical in the bone shell following the ridge contour. The autogenous particles were packed into the space between the split bone block and the ridge. Collagen sponge was used to cover the donor site. After 4 months the site was approached for implant placement using crestal incision

Sponsors

hossam samy mohamed saleh
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
30 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* Patient with missing anterior mandibular teeth * horizontal bone width \< 5 mm * Adequate zone of keratinized tissue

Exclusion criteria

* Presence of infection or periapical lesions in adjacent teeth * Medically compromised patients with a condition that affect the procedure * Insufficient inter-arch distance * Bruxism or clenching * Alcoholism * Smokers

Design outcomes

Primary

MeasureTime frameDescription
Postoperative Painup to 2 weeksIt was assessed through a 10-point Visual Analogue Scale (VAS). The categories were as follows (0-1= None, 2-4= Mild, 5-7= Moderate, 8-10= Severe)
Implant stabilityup to 3 monthsImplant stability was measured using Osstell. Osstell measures the resonance frequency which indicated the implant stability. It has a scale from 1 to 100 where: * \<60 is considered low stability. * 60 \ 69 is considered intermediate stability. * ≥ 70 is considered high stability
Amount of horizontal bone gainup to 4 monthsThis was measured on cone beam computed tomography (CBCT) by comparing pre- and post-operative bone width at specific levels around the implant.

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 13, 2026