Pontic Shield and Mineralized Plasmatic Matrix for Ridge Preservation

NCT ID: NCT07171879

Last Updated: 2025-09-17

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

56 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-09-01

Study Completion Date

2025-07-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This study is testing new methods to preserve the jawbone and gum tissue after removing a damaged front tooth. Normally, when a tooth is taken out, the bone and gums in that area shrink, which can make future dental treatment more difficult and affect appearance. A technique called Partial Extraction Therapy (Pontic Shield Technique) keeps part of the tooth root in place to help maintain the natural shape of the bone and gums. Another method, called Mineralized Plasmatic Matrix (MPM), uses a patient's own blood mixed with bone particles to support healing.

In this randomized clinical trial, 56 patients were assigned to one of four groups:

Group I: Tooth extraction only Group II: Tooth extraction with MPM grafting Group III: Pontic shield technique alone Group IV: Pontic shield technique with MPM grafting The main outcome measured was the amount of bone width preserved, using 3D X-rays (CBCT). Other outcomes included bone height and soft-tissue healing over 4 months.

This research will help determine whether the pontic shield technique, with or without MPM, provides better preservation of bone and gum tissue compared to tooth extraction alone.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Alveolar Ridge Preservation

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Participants were randomized to one of four groups: extraction alone, extraction with MPM, pontic shield alone, or pontic shield with MPM.
Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Extraction Only

Patients receive total tooth extraction in the esthetic maxillary zone without any adjunctive grafting.

Group Type ACTIVE_COMPARATOR

Tooth Extraction only

Intervention Type PROCEDURE

Conventional atraumatic extraction of the non-restorable maxillary tooth in the esthetic zone without socket preservation procedures.

Extraction + MPM

Patients receive total tooth extraction in the esthetic maxillary zone, followed by grafting with MPM.

Group Type ACTIVE_COMPARATOR

Extraction + MPM

Intervention Type PROCEDURE

Tooth extraction followed by socket grafting using MPM, prepared from autologous blood combined with xenograft bone particles.

Pontic Shield Only

Patients undergo the pontic shield technique, in which a portion of the buccal root is preserved to maintain ridge contour, without grafting.

Group Type ACTIVE_COMPARATOR

Pontic Shield Only

Intervention Type PROCEDURE

Partial extraction therapy using the pontic shield technique, in which the buccal root fragment is preserved to maintain ridge contour, without additional grafting.

Pontic Shield + MPM

Patients undergo the pontic shield technique combined with MPM grafting for ridge preservation.

Group Type ACTIVE_COMPARATOR

Pontic Shield + MPM

Intervention Type PROCEDURE

Pontic shield technique combined with grafting using mineralized plasmatic matrix (MPM) for enhanced ridge preservation and healing.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Tooth Extraction only

Conventional atraumatic extraction of the non-restorable maxillary tooth in the esthetic zone without socket preservation procedures.

Intervention Type PROCEDURE

Extraction + MPM

Tooth extraction followed by socket grafting using MPM, prepared from autologous blood combined with xenograft bone particles.

Intervention Type PROCEDURE

Pontic Shield Only

Partial extraction therapy using the pontic shield technique, in which the buccal root fragment is preserved to maintain ridge contour, without additional grafting.

Intervention Type PROCEDURE

Pontic Shield + MPM

Pontic shield technique combined with grafting using mineralized plasmatic matrix (MPM) for enhanced ridge preservation and healing.

Intervention Type PROCEDURE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Adults (≥18 years).
* Classified as ASA I (healthy) according to the American Society of Anesthesiologists Physical Status Classification.
* Presence of Type 1 extraction sockets (intact buccal bone and soft tissues).
* Adequate oral hygiene.
* Sufficient inter-arch space for prosthetic rehabilitation.
* Willingness to comply with study protocol and follow-up schedule.

Exclusion Criteria

* Systemic conditions affecting bone metabolism or wound healing (e.g., uncontrolled diabetes, osteoporosis, immunosuppression).
* History of head and neck radiotherapy or bisphosphonate therapy.
* Acute infection or suppuration at the extraction site.
* Severe periodontal disease.
* Root caries or tooth mobility.
* Buccal bone plate loss due to vertical/horizontal root fractures or advanced periodontitis.
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Soaad Tolba Mohammed Tolba Badawi

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Soaad Tolba Mohammed Tolba Badawi

Lecturer of Oral and Maxillofacial Surgery, Faculty of Dentistry, Mansoura University

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Soaad Tolba Badawy, Lecturer, Oral Surgery, MU

Role: PRINCIPAL_INVESTIGATOR

Mansoura University

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Faculty of Dentistry, Mansoura University

Al Mansurah, Dakahlia Governorate, Egypt

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Egypt

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

R.25.09.22

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Hyaluronic Acid Gel in Ridge Preservation
NCT06176937 COMPLETED PHASE4