Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID07460076

Clinical and Esthetic Outcomes of Immediate Implant Placement With Autogenous Maxillary Tuberosity Graft in the Esthetic Zone: A Prospective Case Series

Led by University of Medicine and Pharmacy at Ho Chi Minh City · Updated on 2026-03-10

15

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Immediate implant placement in the esthetic zone can often lead to buccal bone deficiency, which might affect the long-term stability of the implant and esthetic results. Researchers are studying the use of an autogenous bone graft taken from the maxillary tuberosity to rebuild the buccal bone plate during immediate implant placement. This prospective case series aims to assess clinical and esthetic outcomes such as buccal bone thickness, facial soft tissue thickness, and the pink esthetic score after implant restoration. Participants in this study will receive immediate implant placement in the maxillary esthetic zone along with a two-layer autogenous graft harvested from the maxillary tuberosity. This graft includes cortical bone and connective tissue and is used to reconstruct the buccal bone plate. The study focuses on evaluating how this procedure affects peri-implant tissue stability and esthetic outcomes. Throughout the study, clinical and radiographic evaluations will be performed. Buccal bone thickness will be measured using cone-beam computed tomography (CBCT), while facial soft tissue thickness will be assessed clinically. Esthetic outcomes will be evaluated by the pink esthetic score after the final prosthetic restoration. The primary measurement is buccal bone thickness at six months post-implant placement. Participants will be monitored during follow-up visits to assess these outcomes.

CONDITIONS

Brief Title

Immediate Implant Placement With Autogenous Maxillary Tuberosity Graft in the Esthetic Zone

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Single day procedure with follow-up care

Participants receive immediate implant placement in the maxillary esthetic zone combined with an autogenous bone graft harvested from the maxillary tuberosity to reconstruct the buccal bone plate and improve peri-implant tissue stability and esthetic outcomes.

1 treatment visit and approximately 6 post-operative visits

Follow-up

Duration - 6 months

Clinical and radiographic outcomes are assessed, including buccal bone thickness and facial soft tissue thickness, to evaluate treatment effectiveness and esthetic outcomes.

Multiple follow-up visits over 6 months

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

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Research Team

D

Duy Anh Tran, DDS

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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