Could a sonic wand make root canals less painful?
NCT ID NCT07062419
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether using a sonic device (EndoActivator) to clean the tooth during a root canal reduces pain afterward. Fifty-eight adults with tooth infections were randomly assigned to get either the sonic cleaning or standard syringe irrigation. Pain was measured before and at several times after the procedure using a simple 0-10 scale.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- EndoActivator device
- What this could lead to
- If it works, this could offer a simple way to reduce pain after root canal treatment.
- What could go wrong
- This is a small, completed study with only 58 participants, so results may not apply to everyone. The device may not significantly reduce pain compared to standard care.
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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58 people
The number who actually took part.
- Started
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Jan 2025
- Finished
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Aug 2025
- 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 60 years
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * irreversible pulpitis * symptomatic apical periodontitis * asymptomatic apical periodontitis * compliant patients * sufficient ferrule for post operative restoration Exclusion Criteria: * periapical abcess * severe periodontal disease with guarded periodontal prognosis * teeth with guarded post operative restoration prognosis * non compliant patients
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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
-
28 Military Dental Centre
Lahore, Punjab Province, Pakistan
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Other studies related to the condition(s) this trial covers.
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