Anterior Maxilla Augmentation Using Chin Bone Ring With Implant Placement

Sponsor
Cairo University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05620459
Collaborator
(none)
10
1
1
14
0.7

Study Details

Study Description

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).

Condition or Disease Intervention/Treatment Phase
  • Procedure: Ridge augmentation using chin bone ring with simultaneous implant placement
N/A

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
Anticipated Enrollment :
10 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Computer Guided Simultaneous Implant Placement With Ridge Augmentation Using Autogenous Bone Ring Transplant in Defective Maxillary Anterior Sockets
Actual Study Start Date :
Oct 1, 2022
Anticipated Primary Completion Date :
Oct 1, 2023
Anticipated Study Completion Date :
Dec 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Interventional arm (Ridge augmentation with simultaneous implant placement)

Chin bone ring is harvested using surgical guide to augment anterior maxillary defective recent extraction sockets OR remaining roots that need extraction and are accompanied with labial bone loss Associated with simultaneous implant placement with the aid of surgical guides

Procedure: Ridge augmentation using chin bone ring with simultaneous implant placement
surgical guides are to be used to harvest chin bone ring, the rings are to be used for bone augmentation in extraction sockets (salama and salama classsification type II),simultaneously implant placement.

Outcome Measures

Primary Outcome Measures

  1. Bone quantity (crestal bone) height) [3 months after operation day]

    Cone beam

Secondary Outcome Measures

  1. Bone quality (bone density at the ring alveolus interface) [3 months after operation day]

    In Hounsfield units making use of ROI region of intrest tool included in the software

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 60 Years
Sexes Eligible for Study:
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 cairo University Cairo cairo/Manial Egypt 11553

Sponsors and Collaborators

  • Cairo University

Investigators

  • Principal Investigator: Mostafa M gad, bds, Cairo University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Mostafa Mohamed Gad Mohamed Gad, principal investigator (Master of science student oral and maxillofacial surgery), Cairo University
ClinicalTrials.gov Identifier:
NCT05620459
Other Study ID Numbers:
  • 10722
First Posted:
Nov 17, 2022
Last Update Posted:
Nov 17, 2022
Last Verified:
Nov 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Nov 17, 2022