Skip to main content
Clinical Trials/NCT06566287
NCT06566287
Completed
N/A

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

Hams Hamed Abdelrahman1 site in 1 country22 target enrollmentJanuary 17, 2023

Overview

Phase
N/A
Intervention
Not specified
Conditions
Dental Implant
Sponsor
Hams Hamed Abdelrahman
Enrollment
22
Locations
1
Primary Endpoint
Change in implant stability
Status
Completed
Last Updated
last year

Overview

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.

Registry
clinicaltrials.gov
Start Date
January 17, 2023
End Date
December 19, 2023
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Hams Hamed Abdelrahman
Responsible Party
Sponsor Investigator
Principal Investigator

Hams Hamed Abdelrahman

Assistant Lecturer of Dental Public Health and biostatistical consultanat

Alexandria University

Eligibility Criteria

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

Outcomes

Primary Outcomes

Change in implant stability

Time Frame: 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 Outcomes

  • Change in bone density(Baseline and 3 months)
  • change in thickness of the facial cortical plate(Baseline and 3 months)

Study Sites (1)

Loading locations...

Similar Trials