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Jawbone graft may boost dental implant success in front teeth

NCT ID NCT07460076

Disease control Sponsor: University of Medicine and Pharmacy at Ho Chi Minh City Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study looks at whether using a small piece of bone from the back of the jaw (maxillary tuberosity) can help rebuild the bone around a dental implant placed immediately after a tooth is pulled in the front of the mouth. Researchers will measure bone thickness, gum thickness, and appearance in 15 adults. The goal is to see if this technique leads to better long-term stability and a more natural look.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
autogenous maxillary tuberosity bone graft
What this could lead to
If successful, this approach could improve the stability and appearance of dental implants placed right after tooth extraction in the front of the mouth.
What could go wrong
This is a very small, early study with only 15 participants and no comparison group, so results may not apply widely. Risks include graft failure, infection, or implant loss.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 15 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jan 2026

Expected to finish

Nov 2026

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

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

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Conditions

The condition(s) this trial relates to.

Alveolar Bone Loss periodontal disorder

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Alveolar bone loss Esthetic zone implant rehabilitation

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • University of Medicine and Pharmacy at Ho Chi Minh City

    RECRUITING

    Ho Chi Minh City, Ho Chi Minh, 700000, Vietnam

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