Can your own tooth be the best bone graft? a trial puts it to the test
NCT ID NCT07723183
First seen Jul 23, 2026 · Last updated Jul 29, 2026 · Updated 3 times
Summary
This trial tests whether a bone graft made from a patient's own extracted wisdom tooth works as well as a synthetic material (EthOss) for preserving bone and gum after lower wisdom tooth removal. In a split-mouth design, each participant receives both grafts—one in each socket—and is followed for 24 weeks. Researchers measure pain, swelling, gum healing, and new bone growth to see which material performs better.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- auto tooth bone graft (ATB) or synthetic EthOss
- What this could lead to
- If successful, this could show that using a patient's own tooth as a graft is a safe and effective option for preserving bone and gum after wisdom tooth removal.
- What could go wrong
- This is a small, early-phase trial with only 12 participants, so results may not apply to everyone. Both grafts are already used clinically, so the main question is about comparative performance, not a breakthrough.
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
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
12 people
The number who actually took part.
- Started
-
Aug 2023
- Finished
-
Oct 2025
- 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 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 Hide 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: * Patient who requires surgical removal of bilateral impacted M3. * Patient with impacted bilateral M3 which are sound. * Impacted bilateral M3 classified as Class I or II with Level A or B according to Pell and Gregory's classification. * Presence of M2 adjacent to the M3 to be extracted. * Patient aged 18 to 35 years old. * Patient with periodontal status of: * Basic Periodontal Score (BPE) 2 at lower right and lower left sextants. * Full mouth plaque score \<30%. Exclusion Criteria: * Impacted M3 associated in the following conditions: * Fracture of angle of mandible. * Radiological evidence of cyst or tumour. * Incomplete root formation. * Acute pulpitis or severe pericoronitis that is not under-controlled. * Gross dental caries. * Retained roots of mandibular third molar with history of removal of unerupted/impacted M3. * Patient's age \<18 years old or \> 35 years old * M2 with periapical inflammation, periodontitis, distal caries or delayed or non-responsive pulp sensibility test to exclude tooth with perio-endo lesion. * Pregnant woman. * Patient on oral contraceptives. * Current or previous bisphosphonate therapy or history of radiotherapy to the jaws. * Active smoker.
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Faculty of Dentistry Universiti Malaya
Kuala Lumpur, Wilayah Perseketuan Kuala Lumpur, 50603, Malaysia
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