NCT07239193

Brief Summary

When a tooth is removed, the bone around it (called the alveolar ridge) naturally shrinks. This study compares two bone grafting materials to find out which one better preserves bone after molar extraction: Demineralized Dentin Matrix (DDM): A material made from the patient's own extracted tooth, treated to remove minerals while keeping bone-forming proteins. Mineralized Plasmatic Matrix (MPM): A mixture of a standard bone substitute and platelet-rich plasma from the patient's blood.

Trial Health

63
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
24

participants targeted

Target at below P25 for not_applicable

Timeline
6mo left

Started Dec 2025

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress47%
Dec 2025Nov 2026

First Submitted

Initial submission to the registry

November 16, 2025

Completed
4 days until next milestone

First Posted

Study publicly available on registry

November 20, 2025

Completed
11 days until next milestone

Study Start

First participant enrolled

December 1, 2025

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2026

Expected
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2026

Last Updated

November 20, 2025

Status Verified

November 1, 2025

Enrollment Period

7 months

First QC Date

November 16, 2025

Last Update Submit

November 16, 2025

Conditions

Keywords

socket preservationalveolar ridge preservationDDMdemineralized dentin matrixMPMmineralized plasmatic matrix

Outcome Measures

Primary Outcomes (1)

  • Change in Alveolar Ridge Width

    Measurement of horizontal bone width at the extraction site using cone-beam computed tomography (CBCT).

    Baseline (immediately postoperative) and 4 months postoperatively.

Secondary Outcomes (3)

  • Change in Alveolar Ridge Height

    Baseline (immediately postoperative) and 4 months postoperatively.

  • Change in Bone Density

    Baseline (immediately postoperative) and 4 months postoperatively.

  • Postoperative Pain

    2 days, 1 week, and 1 month postoperatively.

Study Arms (2)

Demineralized Dentin Matrix (DDM) + Platelet-Rich Fibrin (PRF)

EXPERIMENTAL

Participants in this group will receive socket grafting using Demineralized Dentin Matrix (DDM) prepared from their own extracted tooth. The dentin is cleaned, ground into particles, demineralized using 0.6 N hydrochloric acid, rinsed with saline, and mixed with autologous Platelet-Rich Fibrin (PRF) before being placed into the extraction socket. The socket is then closed with resorbable sutures for healing.

Biological: Demineralized Dentin Matrix (DDM) + Platelet-Rich Fibrin (PRF)

Mineralized Plasmatic Matrix (MPM)

ACTIVE COMPARATOR

Participants in this group will receive socket grafting using a Mineralized Plasmatic Matrix (MPM) composed of a commercially available xenograft mixed with Platelet-Rich Plasma (PRP). The mixture forms a cohesive mineralized matrix that is placed into the extraction socket and stabilized with sutures.

Biological: Mineralized Plasmatic Matrix (MPM)

Interventions

Autogenous dentin-derived grafting material is used as a bone substitute for alveolar ridge preservation following molar extraction. PRF, obtained from the patient's centrifuged blood, is mixed with DDM to enhance graft stability and promote healing.

Demineralized Dentin Matrix (DDM) + Platelet-Rich Fibrin (PRF)

A xenogenic bone substitute is mixed with autologous platelet-rich plasma to form a mineralized plasmatic matrix, which serves as a control graft for ridge preservation after molar extraction.

Mineralized Plasmatic Matrix (MPM)

Eligibility Criteria

Age18 Years - 55 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • \- Non-restorable tooth indicated for extraction Multi-rooted teeth Age group of 18 to 55 years Patients free from any systemic disease that may affect bone healing.

You may not qualify if:

  • \- Pregnant females Active infection at extraction site Smokers Systemic conditions affecting healing (e.g. diabetes, medications as bisphosphonates...) Poor oral hygiene. Patient with systemic disease that may affect bone healing. o Uncooperative patient.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Faculty of Dentistry, Cairo University - Department of Oral and Maxillofacial Surgery

Cairo, 12613, Egypt

Location

MeSH Terms

Interventions

Demineralized Dentin MatrixDDMS

Study Officials

  • Tarek Ibrahim ElGhareeb, Phd

    Department of Oral and Maxillofacial Surgery, Faculty of Dentistry, Cairo University

    STUDY CHAIR
  • Salah Eldin ElAbbasy, Phd

    Department of Oral and Maxillofacial Surgery, Faculty of Dentistry, Cairo University

    STUDY DIRECTOR
  • Ahmed Suliman Ahmed, Bds

    Department of Oral and Maxillofacial Surgery, Faculty of Dentistry, Cairo University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
DOUBLE
Who Masked
PARTICIPANT, OUTCOMES ASSESSOR
Masking Details
Single-blind design - participants will not be informed which grafting material (DDM or MPM) was used in their treatment. The operating surgeons and data analysts will be aware of the allocation due to the nature of the procedures.
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Participants will be randomly assigned to one of two parallel groups in a 1:1 ratio. Group A will receive socket grafting with autogenous Demineralized Dentin Matrix (DDM) mixed with Platelet-Rich Fibrin (PRF), while Group B will receive Mineralized Plasmatic Matrix (MPM) composed of xenograft mixed with Platelet-Rich Plasma (PRP). Each participant will receive only one type of intervention.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Dr

Study Record Dates

First Submitted

November 16, 2025

First Posted

November 20, 2025

Study Start

December 1, 2025

Primary Completion (Estimated)

July 1, 2026

Study Completion (Estimated)

November 1, 2026

Last Updated

November 20, 2025

Record last verified: 2025-11

Locations