Skip to content

Mineralized Dentin Graft Versus Beta-Tricalcium Phosphate for Alveolar Ridge Preservation

From Tooth to Bone: Can Mineralized Dentin Graft Be a Viable Alternative to Beta-Tricalcium Phosphate for Alveolar Ridge Preservation? A Randomized Controlled Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07812610
Enrollment
22
Registered
2026-09-10
Start date
2025-01-01
Completion date
2026-01-01
Last updated
2026-09-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alveolar Bone Loss

Keywords

Mineralized Dentin Graft, Autogenous Tooth-Derived Graft, Beta-Tricalcium Phosphate, Tooth Extraction, Cone-Beam Computed Tomography, Histomorphometry, Alveolar Ridge Preservation

Brief summary

The goal of this clinical trial was to compare three ways of helping the jawbone heal after removal of a tooth. The jawbone that supports a tooth is called the alveolar ridge. This bone can become narrower after a tooth is removed. Participants were randomly assigned to one of three groups. One group received no bone graft material. One group received mineralized dentin graft made from the participant's extracted tooth. One group received beta-tricalcium phosphate, which is a synthetic bone graft material. Participants had cone-beam computed tomography, a three-dimensional dental X-ray, immediately after tooth removal and again after 6 months. During dental implant placement at 6 months, researchers collected a small bone sample to examine healing.

Detailed description

After tooth extraction, the alveolar ridge undergoes natural remodeling that can reduce its width and affect future dental implant placement. Alveolar ridge preservation aims to limit these dimensional changes. This randomized controlled clinical trial compared autogenous mineralized dentin graft, beta-tricalcium phosphate, and healing without bone graft material following extraction of hopeless maxillary teeth. Participants were randomly assigned in a 1:1:1 ratio to three groups. The control group received no bone graft material. The mineralized dentin graft group received graft particles prepared from the participant's extracted tooth. The beta-tricalcium phosphate group received a synthetic bone graft material. Alveolar ridge width was measured using cone-beam computed tomography immediately after extraction and at 6 months. During delayed dental implant placement at 6 months, a small bone-core sample was collected from each study site.

Interventions

PROCEDUREAlveolar Ridge Preservation With Autogenous Mineralized Dentin Graft

Following atraumatic tooth extraction, an autogenous mineralized dentin graft prepared chairside from the participant's extracted tooth is placed in the extraction socket.

PROCEDUREAlveolar Ridge Preservation With Beta-Tricalcium Phosphate

Following atraumatic tooth extraction, beta-tricalcium phosphate granules are placed in the extraction socket.

PROCEDUREExtraction Socket Healing Without Bone Graft

Following atraumatic tooth extraction, no bone graft material is placed in the extraction socket.

Sponsors

Soaad Tolba Mohammed Tolba Badawi
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Outcomes Assessor)

Masking description

Participants and the radiographic and histomorphometric outcome assessors were masked to group assignment. The statistician was also masked. The operating surgeon could not be masked and learned the group assignment after tooth extraction when the sealed allocation envelope was opened.

Intervention model description

Three-arm, parallel-group randomized controlled trial in which extraction sites were allocated in a 1:1:1 ratio to healing without bone graft material, autogenous mineralized dentin graft, or beta-tricalcium phosphate.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Aged 18 years or older. * Clinical indication for extraction of a hopeless maxillary tooth. * No evidence of acute infection at the intended extraction site. * Willing and able to comply with the scheduled study visits and follow-up procedures. * Provided written informed consent.

Exclusion criteria

* Systemic disorder known to impair bone metabolism. * History of radiotherapy involving the head and neck region. * Pregnancy or lactation. * Advanced periodontal disease.

Design outcomes

Primary

MeasureTime frameDescription
Change in Alveolar Bone Width From Baseline to 6 MonthsBaseline immediately after tooth extraction and 6 monthsAlveolar bone width was measured in millimeters using cone-beam computed tomography immediately after tooth extraction and at 6 months. Width was measured horizontally from the outer buccal cortical surface to the palatal cortical surface.

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Sep 18, 2026