Clinical and Radiographic Evaluation of Delayed Dental Implant Placement After Socket Preservation Using Injectable Bone Graft

ConditionsAlveolar Ridge Preservation Dental Implant Placement

Trial statusNot yet recruiting

Trial phaseNot applicable

Trial typeInterventional

Biological sexAll

Age40-60

SponsorSuez Canal University

About this trial

This clinical study aims to evaluate the clinical and radiographic outcomes of delayed dental implant placement following socket preservation using an injectable alloplastic bone graft material.

The study will include patients who require tooth extraction and are candidates for implant placement.

After tooth extraction, the socket will be preserved using the bone graft material, and dental implants will be placed after a healing period.

Clinical and radiographic assessments will be performed to evaluate bone quality, bone height, and implant stability.

The goal of this study is to determine the effectiveness of injectable alloplastic bone grafts in maintaining the alveolar ridge and improving the success of delayed implant placement.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Patient aged between 40 and 60 years

General good health.

Volunteer subjects have to voluntarily sign an informed consent.

Patient Indicated for single implant placement in lower posterior area.

Disqualifiers

Patient with systemic disease affection bone metabolism .

Patients with contraindication to surgical treatment.

Patients with uncontrolled medical conditions.

Trial design

Design model

Parallel

Treatments tested in this trial

Injectable Alloplastic Bone Graft
Device
Following tooth extraction, socket preservation will be performed using an injectable alloplastic bone graft material composed of biocompatible synthetic components. The material will be placed into the extraction socket to maintain ridge dimensions and promote bone regeneration. After a healing period of several months, delayed implant placement will be performed, and clinical and radiographic evaluations will assess ridge preservation and implant success

Treatment groups

20 Participants

are divided into 2 treatment groups

Group A: Control GroupNo intervention 0 interventions

Group B: Study GroupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

Implant stability at the time of delayed implant placement

Implant stability will be assessed at the time of delayed implant placement using resonance frequency analysis (RFA) to obtain implant stability quotient (ISQ) values. The ISQ readings will be used to evaluate the effect of socket preservation with injectable alloplastic bone graft on implant stability in comparison to sites without grafting.

Time frame

At the time of delayed implant placement (approximately 4 to 6 months after tooth extraction)

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Suez Canal University

Lead sponsor

Source ClinicalTrials.gov

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