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

Suez Canal University

Status: Not yet enrolling

Conditions: Dental Implant Placement; Alveolar Ridge Preservation

Treatments: Device: Injectable Alloplastic Bone Graft

Study type: Interventional

Funder types: Other

Identifiers

NCT07373600

1004/2025

Details and patient eligibility

About

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.

Enrollment: 20 estimated patients

Sex: All

Ages: 40 to 60 years old

Volunteers: Accepts Healthy Volunteers

Inclusion and exclusion criteria

• 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.

Inclusion criteria for patients in group I

· Patient with a previously extracted lower posterior tooth and the socket was preserved with injectable bone graft .

Exclusion criteria:

• Patient with systemic disease affection bone metabolism .
• Patients with contraindication to surgical treatment.
• Patients with uncontrolled medical conditions.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

---

20 participants in 2 patient groups

Control Group

No Intervention group

Description:

Extraction sites left to heal naturally without any bone grafting material before delayed implant placement. Dental implants will be placed after the natural healing period, and clinical and radiographic evaluations will be performed to assess ridge dimensions and implant outcomes

Study Group

Experimental group

Description:

Extraction sockets will be preserved using an injectable alloplastic bone graft material immediately after tooth extraction. After a healing period, delayed implant placement will be performed. Clinical and radiographic measurements will be used to evaluate ridge preservation and implant success.

Treatment:

Device: Injectable Alloplastic Bone Graft