Could a simple injection make root canals less painful?
NCT ID NCT07704398
First seen Jul 15, 2026 · Last updated Jul 16, 2026 · Updated 1 time
Summary
This trial tests whether a corticosteroid injection given before root canal treatment can reduce pain and inflammation afterward. One hundred adults with symptomatic pulpitis (tooth nerve inflammation) are randomly assigned to receive either standard root canal treatment alone or standard treatment plus a submucosal injection of betamethasone and gentamicin. Researchers measure pain levels and inflammatory markers in the gum fluid over four days to see if the injection helps.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a submucosal injection of betamethasone and gentamicin
- What this could lead to
- If effective, this injection could become a standard addition to root canal treatment to reduce pain and speed recovery.
- What could go wrong
- This is a single-center trial with 100 participants, so results may not apply broadly. The injection carries a small risk of allergic reaction or infection.
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
-
100 people
The number who actually took part.
- Started
-
Oct 2023
- Finished
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Apr 2026
- 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 to 65 years
- Sex
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Anyone
- Healthy volunteers
-
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 diagnosed with symptomatic irreversible pulpitis * Presence of spontaneous pain or pain persisting after removal of the stimulus * Teeth indicated for endodontic treatment * Systemically healthy individuals * Patients able to read and sign the informed consent form * Patients able to complete postoperative pain assessment forms * Patients able to attend the 4-day follow-up visit Exclusion Criteria: * Individuals with systemic disease or immunosuppression * Patients with contraindications to corticosteroid or gentamicin use * Pregnant or breastfeeding individuals * Recent use of antibiotics, analgesics, or anti-inflammatory drugs * Presence of advanced periodontal disease in the affected tooth * Presence of acute periapical or periodontal abscess * Teeth with previous endodontic treatment
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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
-
Yelda Erdem Hepşenoğlu
Istanbul, Atakent Mahallesi, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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