Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Cure My Disease

Don't miss your cure!

 Log in / Sign up

Wisdom tooth graft showdown: donor vs. Patient's own dentin

NCT ID NCT06457373

Disease control Sponsor: Horus University 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Aug 19, 2026 · Updated 3 times

Summary

This study tests whether a donor tooth-derived bone graft works as well as a patient's own tooth graft for preserving jawbone after impacted wisdom tooth extraction. Forty adults with similar impacted wisdom teeth on both sides of the jaw will receive one graft type per side. Researchers will measure bone height and width using special tools and CT scans to see which graft better maintains the socket.

What this could mean

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

Active substance
Demineralized dentin graft (from donor or patient's own tooth)
What this could lead to
If it works, this could point toward a reliable way to preserve jawbone after tooth extraction, potentially improving future dental implant success.
What could go wrong
This is a small, early-stage study with only 40 participants. It may not show a clear difference between the two graft types, and results may not apply to other teeth or patients.

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 40 people

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

Started

Aug 2026

Expected to finish

Aug 2027

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

25 to 35 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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: 1. Patients aged between 25 to 35 years old. 2. Patients scored as (ASA I). 3. No adverse habits such as smoking, tobacco chewing, alcohol. 4. Patients having bilaterally impacted mandibular third molar with similar degree of difficulty according to (Kim JY, et al). 5. The recipient alveolar sockets are free of any pre-existing periapical pathology, based on x-ray. 6. Alveolar sockets with a depth of 5 mm or more, using periodontal probe for assessment. 7. Patients sign a consent for all procedures. Exclusion Criteria: * 1\) Pregnant or lactating patients. 2) Relevant systemic diseases. 3) Patients with history of chemotherapy or radiotherapy.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Alveolar bone loss are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

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

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

  • Faculty of Dentistry- Horus University in Egypt

    RECRUITING

    Damietta, New-Damietta, 34518, Egypt

More trials for these conditions

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