Could a tooth's own pulp be used to regenerate root canals?
NCT ID NCT03833401
First seen Jul 23, 2026 · Last updated Jul 24, 2026 · Updated 1 time
Summary
This trial tests whether transplanting a patient's own minced pulp tissue into a cleaned root canal can regenerate living dental pulp. Fifty participants aged 7 to 50 with infected or inflamed teeth will receive either standard root canal treatment or the experimental tissue transplant. The study will track healing, nerve function, and tooth growth over two years.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- transplantation of the patient's own minced pulp tissue into the cleaned root canal
- What this could lead to
- If it works, this could lead to a treatment that regenerates living pulp inside a tooth, potentially saving teeth that would otherwise need extraction.
- What could go wrong
- This is an early-stage trial with a small number of participants. The procedure may not reliably regenerate pulp tissue, and there is a risk of infection or failure of the transplanted tissue.
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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.
- Started
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Feb 2019
- Expected to finish
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Jun 2021
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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7 to 50 years
- Sex
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Anyone
- Healthy volunteers
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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: * Healthy male or female participants at ages of 7 - 50 y.o. presenting with a tooth diagnosed with complete or partial necrosis of the pulp or irreversible pulpitis. * Participants presenting with donor pulp tissue, either from existing deciduous teeth or from permanent teeth treatment planned for extraction, e.g., second premolars for orthodontic extraction or third molars. * Participants presenting with irreversible pulpitis and partial necrosis, i.e., visible pulpal tissues during access opening and canal debridement. * Participants with immature root apices, including those with partially closed apex, that require root canal procedure. Exclusion Criteria: * Participants with any systemic conditions preventing routine dental procedures or requiring medication that interfere with healing or induce bleeding. * Participants with avulsed, replanted teeth with resultant pulp necrosis. * Participants with vertical root fracture/cracks. * Participants with teeth that are not restorable.
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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
-
UCLA School of Dentistry
Los Angeles, California, 90095, United States
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