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Clinical Trials/NCT03394625
NCT03394625
Unknown
Not Applicable

Evaluation of Marginal Bone Loss in Immediate Implant Placement in Maxillary Esthetic Zone Using Socket Shield Technique Versus Xenogenous Bone Substitute Material

Cairo University1 site in 1 country18 target enrollmentJuly 1, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Marginal Bone Loss in Socket Shield Technique
Sponsor
Cairo University
Enrollment
18
Locations
1
Primary Endpoint
marginal bone loss
Last Updated
7 years ago

Overview

Brief Summary

Anterior maxilla (Esthetic zone) is very challenging area because of thin buccal plate of bone. After tooth extraction physiological process occur causing alteration of bone and soft tissue so, delayed placement of implant lead to loss of bone height and width. Immediate placement of implant is become essential to preserve the bone and soft tissue from loss.

Socket shield technique is a recent technique which is by sectioning the root and extraction of palatal part and leaving buccal part of the root with its attachment of periodontal ligament and vascularization still intact then placing implant in palatal socket. This technique allow preservation of buccal plate of bone and soft tissue with minimum loss allowing better result in esthetic zone.

Registry
clinicaltrials.gov
Start Date
July 1, 2017
End Date
December 20, 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Mohammed Ibrahim Shaalan

Principal investigator

Cairo University

Eligibility Criteria

Inclusion Criteria

  • Patients with badly broken teeth in upper esthetic zone with intact periodontal condition indicated for extraction, presence of at least 4 mm of bone beyond the root apex to guarantee implant primary stability, implant placement within the alveoli confines.
  • Both sexes.
  • No intraoral soft and hard tissue pathology.
  • Physically able to tolerate conventional surgical and restorative procedures.
  • Signing of an informed consent form.

Exclusion Criteria

  • Presence of fenestrations or dehiscence of the residual bony walls after extraction.
  • Heavy smokers more than 20 cigarettes per day .(24)
  • Patients with systemic disease that may affect normal healing e.g. uncontrolled diabetes.
  • Psychiatric problems e.g. severe bruxism.
  • Disorders to implant are related to history of radiation therapy to the head and neck neoplasia, or bone augmentation to implant site.
  • Active infection in the teeth to be treated
  • Vertical root fractures with displacement in the teeth of the surgical area

Outcomes

Primary Outcomes

marginal bone loss

Time Frame: 4 months

will be measured from CBCT using Blue-sky software built-in linear measuring tool by millimeters

Study Sites (1)

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