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Your pulled tooth could rebuild your jaw

NCT ID NCT07812610

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Sep 10, 2026 · Last updated Sep 18, 2026 · Updated 3 times

Summary

Researchers compare three ways to preserve the jawbone after a tooth is removed. Participants are randomly assigned to receive no bone graft, a graft made from their own extracted tooth, or a synthetic bone substitute called beta-tricalcium phosphate. The trial measures changes in jawbone width using 3D dental X-rays taken right after extraction and again 6 months later, when a small bone sample is collected during implant placement.

What this could mean

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

Active substance
A bone graft made from the patient's own extracted tooth, compared with a synthetic bone substitute and with no graft
What this could lead to
If the tooth-derived graft works as well as the synthetic material, dentists could reuse a patient's own tooth to preserve jawbone, avoiding a synthetic product.
What could go wrong
The trial is small, with 22 participants, and measures bone width at 6 months. It may not show a clear difference between the three approaches, and longer-term outcomes are unknown.

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

22 people

The number who actually took part.

Started

Jan 2025

Finished

Jan 2026

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: * Aged 18 years or older. * Clinical indication for extraction of a hopeless maxillary tooth. * No evidence of acute infection at the intended extraction site. * Willing and able to comply with the scheduled study visits and follow-up procedures. * Provided written informed consent. Exclusion Criteria: * Systemic disorder known to impair bone metabolism. * History of radiotherapy involving the head and neck region. * Pregnancy or lactation. * Advanced periodontal disease.

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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.

Contacts and locations

Locations

  • Faculty of Dentistry, Mansoura University

    Al Mansurah, Aldakhlia, 35516, Egypt

More trials for these conditions

Other studies related to the condition(s) this trial covers.