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Chilled solution or steroid: which eases Post-Root-Canal pain?
NCT ID NCT07738302
First seen Jul 31, 2026 · Last updated Jul 31, 2026
Summary
This trial tests whether using cold irrigation solutions or adding dexamethasone during root canal treatment can lower post-operative pain in people with symptomatic irreversible pulpitis and acute apical periodontitis. Sixty medically healthy adults aged 20-50 will be randomly assigned to receive one of four irrigation combinations. The study measures pain levels using a visual analogue scale to see if these approaches reduce discomfort after the procedure.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Cold sodium hypochlorite (NaOCl) and dexamethasone, used as irrigation solutions during root canal treatment
- What this could lead to
- If effective, this could offer a simple, drug-sparing way to reduce pain after root canal procedures, potentially improving patient comfort and recovery.
- What could go wrong
- This is a small, early-stage trial, and results may not apply to all patients. Cold irrigation or dexamethasone may not significantly reduce pain compared to standard care, and individual responses can vary.
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 60 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Sep 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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20 to 50 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.
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: * Medically free Patients. (ASA I and II) * Age between 20-50 years old. * Males \& Females. * Patients' acceptance for participating in the trial through an informed consent (Appendix I) * Diagnosed clinically and radiographically with symptomatic irreversible pulpitis with apical peridontitits * No periapical radiolucency * Patent canals with n Exclusion Criteria: Non restorable teeth. * No bleeding upon conducting access preparation. * Teeth presenting with: * History of trauma or 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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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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.
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