Gum disease breakthrough? hyaluronic acid gel may rival standard treatment
NCT ID NCT07230522
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a hyaluronic acid gel (HyaDent BG) works as well as Emdogain, a standard treatment, for repairing bone defects caused by gum disease. Both were used with a bone graft material during surgery. Seventeen adults with advanced periodontitis took part. The goal was to see if the hyaluronic acid could reduce pocket depth, improve gum attachment, and increase bone fill similarly to Emdogain.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- hyaluronic acid gel (HyaDent BG) and enamel matrix proteins (Emdogain)
- What this could lead to
- If hyaluronic acid works as well as Emdogain, it could offer a simpler, possibly cheaper option to help regrow bone lost to gum disease.
- What could go wrong
- This is a very small study (17 people) with no blinding, so results may not hold up in larger trials. Gum disease often requires ongoing care, so this is not a permanent fix.
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
-
17 people
The number who actually took part.
- Started
-
Mar 2024
- Finished
-
Jan 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 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 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: * Adults over the age of 18 diagnosed with periodontal disease-Stage III or IV periodontitis; * Sites with bone defects and a probing pocket depth (PPD) ≥ 6 mm, accompa-nied by bleeding on probing (BoP) at re-evaluation, conducted six weeks after non-surgical periodontal therapy; * Full Mouth Plaque Score (FMPS) \< 20% and Full Mouth Bleeding Score (FMBS) \< 15% prior to surgical treatment; * Good general health with no systemic conditions and no known allergies to materials or medications used in the study. Exclusion Criteria: * Medical conditions contraindicating surgical intervention; * Pregnancy or lactation; * Heavy smokers; * Untreated periodontal disease; * Poor oral hygiene; * Acute infectious lesions in the area of intervention;
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Intrabony periodontal defect are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Departement of Periodontology, Faculty of Dental Medicine, Medical University of Sofia
Sofia, Bulgaria
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Could a pill replace an IV for gum surgery pain relief?
- Can everyday supplements boost gum disease therapy?
- Can pulling a loose tooth and putting it back save it?
- Gum fluid proteins eyed as link between smoking and periodontitis
- Gum fluid holds clues to Behçet's disease puzzle
- Magnifying the fight against gum disease: loupe vs microscope