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

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

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

Treatments tested in this trial

  • Injectable Alloplastic Bone Graft

Treatment groups

20 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators