This study will evaluate the clinical efficacy of injectable alloplastic bone grafts in terms of radiography and histology in order to preserve tooth sockets following extraction. Methodology: Twenty new extraction sockets from twenty surgically extracted non-restorable mandibular molar teeth will be used in this clinical investigation.
Age range
40 Years – 60 Years
Sex
ALL
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The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Change in buccolingual ridge width assessed by CBCT
Timeframe: Baseline and 4 months
Bone density assessed by CBCT
Timeframe: Baseline and 4 months
Percentage of newly formed bone assessed histomorphometrically
Timeframe: 3 months
Percentage of residual graft material
Timeframe: 3 months
Percentage of connective tissue
Timeframe: 3 months