Immediate implant with bone graft taken from the maxillary tuberosity to improve upper front-tooth esthetics.

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This prospective interventional case series combines immediate implant placement in the maxillary esthetic zone with a two-layer autogenous graft harvested from the maxillary tuberosity (cortical bone plus connective tissue). Patients requiring extraction and a single upper-front implant receive the graft at the time of implant placement and are followed with clinical exams and cone-beam CT imaging. Primary outcomes are buccal bone thickness on CBCT, facial soft tissue thickness measured clinically, and the pink esthetic score after definitive restoration. Follow-up assessments will track radiographic and esthetic changes to determine whether the tuberosity graft improves peri-implant tissue stability.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* 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

Exclusion Criteria:

* Uncontrolled sHistory of radiotherapy in the head and neck region ystemic 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

Where it's running

• University of Medicine and Pharmacy at Ho Chi Minh City
  Ho Chi Minh City, Ho Chi Minh, Vietnam Recruiting

Study contacts

• Study coordinator: Duy Anh Tran, DDS
• Email: tranduyanhump17@gmail.com
• Phone: +84 868324216

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.