About this trial
For the first time, allografts from human-extracted teeth will be prepared and evaluated in a prospective clinical trial to assess their efficacy for alveolar ridge preservation. The reconstruction and preservation of the alveolar ridge after tooth extraction are essential for future prosthetic rehabilitation.
Autogenous bone grafts, while effective, are limited by donor site morbidity and insufficient graft quantity. Allogenic dentin grafts from healthy human donors present a scalable solution. This study aims to evaluate the biocompatibility and effectiveness of two types of allogenic dentin grafts-demineralized dentin allografts (DDA) and whole tooth allografts (WTA)-for alveolar ridge preservation, contributing to innovative, sustainable dental practices.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
None
Disqualifiers
Students, interns, or residents willing to participate and provide informed consent.
No history of systemic diseases such as diabetes, hepatitis, or immune disorders.
Negative blood screening for HIV, HBV, and HCV.
Non-smokers or individuals who have not smoked within the last six months.
Trial design
Parallel
Treatments tested in this trial
DDA
Biological/Vaccine: demineralized dentin allografts (DDA) allografts from human extracted teeth will be prepared and evaluated in a prospective clinical trial to assess their efficacy for alveolar ridge preservation. The reconstruction and preservation of the alveolar ridge after tooth extraction are essential for future prosthetic rehabilitation. Autogenous bone grafts, while effective, are limited by donor site morbidity and insufficient graft quantity. Allogenic dentin grafts, derived from healthy human donors, present a scalable solution.
WTA
Biological/Vaccinewhole tooth allografts (WTA) allografts from human extracted teeth will be prepared and evaluated in a prospective clinical trial to assess their efficacy for alveolar ridge preservation. The reconstruction and preservation of the alveolar ridge after tooth extraction are essential for future prosthetic rehabilitation. Autogenous bone grafts, while effective, are limited by donor site morbidity and insufficient graft quantity. Allogenic dentin grafts, derived from healthy human donors, present a scalable solution.
Treatment groups
Trial outcomes
Primary outcomes
Change in alveolar ridge width and height (in mm) from baseline to 3 months post-extraction, measured using CBCT scans.
Secondary outcomes
Change in alveolar crest height and width (in mm) from baseline to 3 months post-extraction, measured using CBCT scans, comparing DDA, WTA, and ungrafted control sites.
Sponsors and contacts
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Jordan University Hospital
Lead sponsor
hanan Jafar
Collaborator