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Clinical Trials/NCT05336149
NCT05336149
Unknown
Not Applicable

Demineralized Whole-tooth vs Demineralized Particulate Dentin Grafts in Alveolar Ridge Preservation. a Randomized Controlled Trial.

Cairo University1 site in 1 country20 target enrollmentJune 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Alveolar Bone Loss
Sponsor
Cairo University
Enrollment
20
Locations
1
Primary Endpoint
Alveolar bone width change in mm
Last Updated
4 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
June 2022
End Date
June 2023
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ahmed Mohamed AbdelRaouf Hussein

Principal investigator

Cairo University

Eligibility Criteria

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
  • systemic conditions affecting healing (e.g. diabetes, medications as bisphosphonates...)

Outcomes

Primary Outcomes

Alveolar bone width change in mm

Time Frame: 6 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 Outcomes

  • Alveolar bone height change in mm(6 months)
  • Histological assessment(6 months)

Study Sites (1)

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