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Demineralized Whole-tooth vs Demineralized Particulate Dentin Grafts in Alveolar Ridge Preservation

Not Applicable
Conditions
Alveolar Bone Loss
Interventions
Procedure: Alveolar ridge preservation using whole-tooth dentin graft
Procedure: Alveolar ridge preservation using particulate dentin graft
Registration Number
NCT05336149
Lead Sponsor
Cairo University
Brief Summary

The aim of this trial is to compare whole-tooth vs particulate dentin for their effects in alveolar ridge preservation.

Detailed Description

Extraction of the teeth is still one of the most commonly undertaken procedures in dental practices due to various reasons that render the teeth non-restorable. Following extraction, replacing the lost teeth with a prosthetic alternative that provides for both optimal esthetics and function can be challenging due to the inevitable events of socket healing that results in the reduction in alveolar bone height and width. To overcome these limitations and provide for adequate ridge volume, different bone preservation or augmentation techniques can be utilized with different clinical applications.

Alveolar ridge preservation is a procedure that attempts to reduce bone dimensional changes that naturally take place following tooth extraction. To overcome this problem, various approaches using various grafting materials and/or covering membranes have been proposed with varied success. The extracted tooth is no longer considered as clinical waste, it has been explored as an appropriate source for autogenous graft substitute. This idea emerged due to the shared embryonic origin of bone and teeth as well as the similarities in chemical structure as dentin is composed of 30-35% organic part and 65-70% inorganic part in comparison to alveolar bone, with inorganic and organic parts of 35% and 65% respectively. Both whole-tooth and particulate forms has been utilized for alveolar ridge preservation or augmentation but the superiority of one form over the other is not yet clear.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
20
Inclusion Criteria
  • Non-restorable tooth indicated for extraction
  • single-rooted teeth
  • Patients at least 18 years or older
  • Motivated patients, agree to sign informed consent and complete the follow-up period
Exclusion Criteria
  • Pregnant females
  • active infection at extraction site
  • Smokers
  • systemic conditions affecting healing (e.g. diabetes, medications as bisphosphonates...)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Whole-tooth dentin graftAlveolar ridge preservation using whole-tooth dentin graftThe extracted tooth will be prepared as whole-tooth dentin graft and inserted in the extraction socket.
Particulate dentin graftAlveolar ridge preservation using particulate dentin graftThe extracted tooth will be prepared as particulate dentin graft and inserted in the extraction socket.
Primary Outcome Measures
NameTimeMethod
Alveolar bone width change in mm6 months

Alveolar bone linear width will be measured at baseline at final cone beam computed tomography (CBCT) scans. The change in bone width will be calculated as the subtraction of final width from baseline width and will be expressed in millimetres.

Secondary Outcome Measures
NameTimeMethod
Alveolar bone height change in mm6 months

Alveolar bone linear height will be measured at baseline at final cone beam computed tomography (CBCT) scans. The change in bone height will be calculated as the subtraction of final height from baseline height and will be expressed in millimetres.

Histological assessment6 months

Bone samples from at least one control and one intervention site will be taken during implant placement using a trephine bur. Samples will be examined for new bone formation (Yes/no) and inflammatory response (Yes/no).

Trial Locations

Locations (1)

Cairo University

🇪🇬

Cairo, Egypt

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