Socket Shield Technique With CGF and Xenograft for Immediate Implants

ConditionsAlveolar Bone Loss Socket Shield Technique Bone Resorption Immediate Dental Implant Placement Concentrated Growth Factors Xenograft Alveolar Bone Preservation

Trial statusNot yet recruiting

Trial phaseNot applicable

Trial typeInterventional

Biological sexAll

Age18+

SponsorCairo University

About this trial

This prospective case series aims to evaluate the clinical and radiographic outcomes of immediate implant placement using the socket shield technique combined with concentrated growth factors (CGF) and xenograft in the esthetic zone. The study will assess crestal bone level changes and implant stability over a 6-month follow-up period.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥18 years old. (Younis, W., & El-Rashidy, A. 2020).

Both male and female patients.

Maxillary, anterior and premolar segments.

Disqualifiers

A medical history that contraindicates oral surgical treatment such as (uncontrolled/untreated diabetes mellitus, immuno-compromised status, radio or chemotherapy of the oral and maxillofacial region, treatment with oral and/or intravenous bisphosphonates).

Presence of active or untreated periodontal disease.

Vertical root fractures involving the buccal aspect.

Tooth /teeth with horizontal fractures below bone level.

Trial design

Design model

Single group

Treatments tested in this trial

Socket Shield Technique with Immediate Implant Placement and CGF + Xenograft
Procedure/Surgery
The procedure involves partial extraction therapy using the socket shield technique, where the buccal portion of the root is preserved to maintain the alveolar bone. Immediate implant placement is performed into the extraction socket. Concentrated growth factors (CGF) are prepared from the patient's autologous blood via centrifugation and combined with xenograft to form a "sticky bone" graft. This graft is placed in the jumping gap between the implant and socket wall to enhance bone regeneration and healing. Implant stability will be measured using resonance frequency analysis (Osstell), and radiographic evaluation will be performed using CBCT.

Treatment groups

7 Participants

are divided into 1 treatment group

Group A: Socket Shield Technique with CGF and Xenograft in Immediate Implant PlacementExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

crestal bone level

Evaluation of changes in crestal bone level around the dental implant using cone-beam computed tomography (CBCT). Measurements will be taken from a fixed reference point on the implant to the first bone-to-implant contact recorded in millimeters (mm)

Time frame

2 weeks, and 6 months postoperatively

Secondary outcomes

Implant Stability (ISQ Values)

Implant stability will be assessed using resonance frequency analysis with the Osstell device and recorded as Implant Stability Quotient (ISQ). ISQ values range from 1 to 100, where higher values indicate greater implant stability and a better outcome.

Time frame

Immediate postoperative, and at 6 months

Sponsors and contacts

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

Cairo University

Lead sponsor

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: