Skip to content

Anterior Maxilla Augmentation Using Chin Bone Ring With Implant Placement

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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05620459
Enrollment
10
Registered
2022-11-17
Start date
2022-10-01
Completion date
2023-12-31
Last updated
2022-11-17

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

Conditions

Ridge Augmentation

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

Interventions

PROCEDURERidge 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.

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 60 Years
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.

Design outcomes

Primary

MeasureTime frameDescription
Bone quantity (crestal bone) height)3 months after operation dayCone beam

Secondary

MeasureTime frameDescription
Bone quality (bone density at the ring alveolus interface)3 months after operation dayIn Hounsfield units making use of ROI region of intrest tool included in the software

Countries

Egypt

Contacts

Primary ContactMostafa M gad, BDS
mostafa.gad@dentistry.cu.edu.eg201000264683

Outcome results

None listed

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