Socket Shield TechniqueConcentrated Growth FactorsImmediate Dental Implant PlacementAlveolar Bone PreservationAlveolar Bone Loss
Investigational drug(s) / intervention(s)
Immediate implant placement with Socket Shield Technique and CGF
Immediate implant placement with Socket Shield Technique and CGF: Partial extraction therapy using the socket shield technique followed by immediate implant placement. Concentrated growth factors prepared from autologous blood will be packed in the jumping gap to enhance bone regeneration and healing.
Study summary
This prospective case series study aims to clinically and radiographically evaluate the effectiveness of the socket shield technique combined with concentrated growth factors (CGF) in immediate implant placement in the esthetic zone. Outcomes will include crestal bone level changes assessed by CBCT and implant stability measured using Osstell.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* Age ≥18 years old. (Younis, W., \& El-Rashidy, A. 2020).
* Both male and female patients.
* Maxillary, anterior and premolar segment.
Exclusion Criteria:
* 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.
* Tooth /teeth with external or internal resorption.
* Patients with destructive oral habits such as smoking, chewing tobacco, bruxism, etcetera.
Primary outcome measure(s)
Crestal bone level — 2 weeks and 6 months post-operatively Radiographic evaluation of crestal bone level changes around the implant using CBCT, measured in millimeters (mm).
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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