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Ridge Splitting Using Autogenous Bone Wedge Versus the Conventional Intercortical Augmentation Technique in Horizontally Deficient Anterior Maxilla

Not Applicable
Recruiting
Conditions
Horizontal Ridge Deficiency
Interventions
Procedure: autogenous bone wedge
Registration Number
NCT06529653
Lead Sponsor
Cairo University
Brief Summary

The current study aimed to evaluate both the quality and quantity of gained and maintained bone width after ridge splitting utilizing autogenic bone wedges versus mixed bone particles for horizontal ridge augmentation in the anterior esthetic zone.

Detailed Description

This randomized clinical study included 20 patients with a horizontally deficient ridge in the esthetic region. Two groups were divided according to the type of intercortical bone graft used after ridge splitting: 10 patients for each. (The intervention group) had grafting with autogenous bone wedges harvested from the chin, and (the control group) had mixed (autogenic and xenogenic) bone particles.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
20
Inclusion Criteria
  1. All patients possessed partially edentulous anterior maxillary ridge with the following criteria

    1. The anterior maxillary vertical dimension was more than ten mm measured from the alveolar crest to the basal bone of the maxilla.
    2. The horizontal alveolar dimension varies from 3-5 mm at the crest and 6-8 mm at the basal part of the ridge measured from the labial cortex to the lingual cortex.
  2. All patients were free from any medical conditions that may affect bone healing .

  3. No local pathosis that may interfere with bone healing.

  4. No previous grafting procedures at the indicated edentulous ridge.

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Exclusion Criteria

1- Patients suffering from any systemic disease that may affect bone healing. 2- Patients with less than 3mm labio palatal alveolar ridge width. 3- Ridge with inadequate vertical bone height. 4- Presence of any local pathosis that may interfere with bone healing. 5- Patients unable to continue the whole follow up.

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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
control groupautogenous bone wedgethe group used mixed autogenic and xenogenic bone particles that interposed between split cortices in anterior maxilla to manage the horizontal deficiency of the ridge
intervention groupautogenous bone wedgethe group using an autogenous bone wedge harvested from the chin interpositioned between split cortices in the anterior maxilla to manage the horizontal deficiency of the ridge.
Primary Outcome Measures
NameTimeMethod
bone width in (mm) by cone beam pre, immediate post operative and 6 months postoperative6 months

after ridge augmentation in both groups, the bone width will be measured immediately postoperatively and 6 months postoperatively with cone beam and the measurements of the three intervals (pre-, immediate and 6 months postoperatively) will be compared in both groups to evaluate the amount of gained and maintained bone width

Secondary Outcome Measures
NameTimeMethod
percentage of areas of new bone (%)6 months

The harvested core biopsies would be stained with H\&E and Massons trichrome stain and be microscopically examined to determine percentage areas of newly formed bone

Trial Locations

Locations (1)

oral and maxillo facial Surgery Department; Faculty of dentistry, Cairo University.

🇪🇬

Cairo, Egypt

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