Immediate and Delayed Implant Placement Using Socket Shield Technique and Autogenous Dentin Graft

Immediate And Delayed Implant Placement Using Socket Shield Technique And Autogenous Dentin Graft (A Randomized Clinical Trial)

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT06566287

Enrollment

Registered

2024-08-22

Start date

2023-01-17

Completion date

2023-12-19

Last updated

2024-08-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dental Implant, Socket Shield, Tooth Loss

Brief summary

One of the techniques that have been proposed to reduce the amount of bone resorption in anterior maxilla is the socket shield (SS) . This technique includes preservation of the facial segment of a root to be extracted and immediate implant placement. A technique of socket shield with delayed implantation using autogenous dentin graft for socket preservation, as an alternative to autogenous bone grafts, has shown predictable clinical and histological outcomes.

Interventions

OTHERImmediate implant

Immediate Implant with Socket Shield Group

OTHERDelayed implant

Delayed Implant with Socket preserved with socket Shield and dentin graft Group

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to 50 Years

Healthy volunteers

Inclusion criteria

* Patients with badly destructed or non-restorable maxillary anterior teeth when the Labial cortical plate is still intact, and the thickness was found to be \<2mm in CBCT. * Patients with health status according to American Society of Anesthesiology (ASA) I and II. * Patients who agree to participate in the study.

Exclusion criteria

* Patients presenting with any systemic pathology or health condition that would inhibit the osseointegration process of the implants. * Perforated labial cortical plate seen in CBCT. * Patients undergoing radiation therapy or history of radiation within the last two years. * Drug or alcohol abuse

Design outcomes

Primary

Measure	Time frame	Description
Change in implant stability	Baseline and 3 months	The stability of each implant will be measured using the Osstell device. The ISQ value will be measured immediately at the time of surgery and after three months

Secondary

Measure	Time frame	Description
change in thickness of the facial cortical plate	Baseline and 3 months	patients will be subjected to CBCT scans
Change in bone density	Baseline and 3 months	patients will be subjected to CBCT scans

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026