Own-Blood gel may ease pain after wisdom tooth removal
NCT ID NCT07153133
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether a gel made from a patient's own blood (albumin platelet-rich fibrin) can reduce pain, swelling, and improve healing after removing impacted wisdom teeth. Sixteen healthy adults had both lower wisdom teeth removed; one socket received the gel and the other did not. Researchers measured swelling, pain, wound healing, and blood markers of inflammation.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- albumin platelet-rich fibrin gel (made from the patient's own blood)
- What this could lead to
- If it works, this could offer a simple, natural way to reduce pain and swelling after wisdom tooth removal.
- What could go wrong
- This is a very small, early study with only 16 people, so results may not apply to everyone. The gel is made from the patient's own blood, so risks are low but 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
-
16 people
The number who actually took part.
- Started
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Sep 2025
- Finished
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Mar 2026
- Lead sponsor
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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 40 years
- Sex
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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 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: * Healthy patients classified as ASA (American Society of Anesthesiologists) Physical Status Classification Class I. * Patients seeking extraction of both mandibular third molars. * Patients aged 18 - 40 years old by the day of surgery. * Patients willing to participate in the study and commit to regular follow-up appointments. Exclusion Criteria: * Heavy Smokers (more than 25 cigarettes per day). * Patients with Poor oral hygiene. * Patients with history of a chemotherapy or radiotherapy
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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, Mansoura Universty
Al Mansurah, Egypt
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