Root canal battle: which medicament kills more bacteria?
NCT ID NCT07671326
First seen Jun 27, 2026 · Last updated Jun 30, 2026 · Updated 2 times
Summary
This study tests two different medicines placed inside root canals to kill bacteria in teeth with chronic infection. 24 adults with infected molars will receive either a bioceramic or a calcium hydroxide paste. Researchers measure bacterial levels before and after treatment to see which works better.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Bio-C Temp (bioceramic) and UltraCal XS (calcium hydroxide)
- What this could lead to
- If one medicament proves more effective at killing bacteria, it could improve success rates for root canal treatments and reduce the need for retreatment.
- What could go wrong
- This is a small, early-stage study with only 24 participants, so results may not apply to all patients. The outcome is based on bacterial levels, not long-term tooth survival.
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
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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
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About 24 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Oct 2025
- Expected to finish
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Dec 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 to 65 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: * Patients aged between 18 and 65 years * Being systemically healthy (ASA I or ASA II) * Mandibular molar teeth with a radiographically detectable radiolucent lesion in the periapical region * Willingness of the volunteer or their legal representative to participate in the study by signing the Informed Consent Form Exclusion Criteria: * Patients who have received antibiotics or corticosteroids within the last 3 months * Patients with systemic diseases * Teeth that cannot be properly isolated with a rubber dam * Teeth with periodontal pockets \>4 mm and teeth with crown/root fractures * Individuals who are undergoing or planning to start orthodontic treatment during the study period * Pregnant or breastfeeding individuals
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Istanbul Medipol University
RECRUITINGIstanbul, Istanbul, 34230, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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