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Clinical Trials/NCT05620459
NCT05620459RecruitingNot Applicable

Computer Guided Simultaneous Implant Placement With Ridge Augmentation Using Autogenous Bone Ring Transplant in Defective Maxillary Anterior Sockets

Cairo University2 sites in 1 country10 target enrollmentStarted: October 1, 2022Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
10
Locations
2
Primary Endpoint
Bone quantity (crestal bone) height)
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

The study aims toward using autogenous bone grafts to solve decreased bone quantity in anterior maxilla while allowing the patient to recieve implants simultaneously (same time of grafting).

Detailed Description

  • Chin bone ring will be harvested from patient's(10 in number) chin to augment the recent extraction socket with buccal bone defect, followed by implant placement.
  • The process of harvesting and placement of ring will be computer guided which adds lots of accuracy to the bone ring required size from the donor site and the proper placement of both the ring and the implant at the recipient site

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
20 Years to 60 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •Patients with non-restorable teeth in the maxillary anterior region with insufficient buccal bone height or buccal bone defect.
  • •Patients who have given their consent for this trial.
  • •Both genders males and females will be included.

Exclusion Criteria

  • •• Untreated periodontitis.
  • •Poor oral hygiene and motivation.
  • •Uncontrolled diabetes.
  • •Pregnant or nursing.

Outcomes

Primary Outcomes

Bone quantity (crestal bone) height)

Time Frame: 3 months after operation day

Cone beam

Secondary Outcomes

  • Bone quality (bone density at the ring alveolus interface)(3 months after operation day)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Mostafa Mohamed Gad Mohamed Gad

principal investigator (Master of science student oral and maxillofacial surgery)

Cairo University

Study Sites (2)

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