Actively Recruiting
Immediate Implant Placement With Autogenous Maxillary Tuberosity Graft in the Esthetic Zone
Led by University of Medicine and Pharmacy at Ho Chi Minh City · Updated on 2026-03-10
15
Participants Needed
1
Research Sites
43 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Immediate implant placement in the esthetic zone is often associated with buccal bone deficiency, which may compromise esthetic outcomes and long-term implant stability. Autogenous bone graft harvested from the maxillary tuberosity provides corticocancellous bone with favorable biological properties and may help reconstruct the buccal bone plate during immediate implant placement. This prospective case series aims to evaluate the clinical and esthetic outcomes of immediate implant placement combined with autogenous maxillary tuberosity graft in the esthetic zone. The primary outcomes include buccal bone thickness measured on cone-beam computed tomography (CBCT), facial soft tissue thickness measured clinically, and the pink esthetic score (PES) after implant restoration.
CONDITIONS
Official Title
Immediate Implant Placement With Autogenous Maxillary Tuberosity Graft in the Esthetic Zone
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 18 years or older
- Patients requiring single implant placement in the maxillary esthetic zone
- Indication for immediate implant placement following tooth extraction
- Presence of a buccal bone defect requiring augmentation with an autogenous maxillary tuberosity bone graft
- Adequate oral hygiene and ability to maintain postoperative care
- Willingness to participate in the study and provide informed consent
You will not qualify if you...
- Uncontrolled systemic diseases
- History of radiotherapy in the head and neck region
- Active periodontal disease or untreated oral infection
- Heavy smoking (more than 10 cigarettes per day)
- Pregnancy or lactation
- Severe parafunctional habits
- Insufficient bone volume preventing implant placement with the planned protocol
- Patients unable to attend follow-up visits
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of Medicine and Pharmacy at Ho Chi Minh City
Ho Chi Minh City, Ho Chi Minh, Vietnam, 700000
Actively Recruiting
Research Team
D
Duy Anh Tran, DDS
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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