New gum repair gel takes on gold standard in Tooth-Saving showdown
NCT ID NCT07430748
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This early-phase study tests whether a new biomaterial (REGENFAST) works better than a standard platelet-based treatment (L-PRF) for repairing gum and bone damage caused by gum disease. Fifteen adults with matching defects on both sides of the mouth will receive one treatment on each side, and healing will be compared over 3 months. The goal is to see which material better restores tooth support and improves gum health.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Early phase 1
The earliest testing in people: a first look at safety, in a very small group.
- Participants
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About 15 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2026
- Expected to finish
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May 2026
An estimate. End dates often move.
- 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
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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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: * Adult patients (≥18 years old) in good general health (ASA I-II). * Bilateral gingival recessions or symmetrical bone defects. * Absence of active infection or inflammation. * Good oral hygiene level (Plaque Index \<20%). * Signed informed consent and commitment to follow-up. Exclusion Criteria: * Systemic diseases that impair healing (uncontrolled diabetes, immunodeficiency, etc.). * Periodontal or antibiotic treatment within the last 6 months. * Smokers (\>10 cigarettes/day). * Pregnancy or breastfeeding. * Allergy or hypersensitivity to REGENFAST® or surgical materials. * Use of medication affecting healing (corticosteroids, immunosuppressants, bisphosphonates). * Lack of availability to attend follow-up visits.
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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
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Facultade de Odontoloxía
Santiago de Compostela, A Coruña, 15782, Spain
More trials for these conditions
Other studies related to the condition(s) this trial covers.