Can a steroid injection before root canal silence Post-Procedure pain?
NCT ID NCT07755306
First seen Aug 10, 2026 · Last updated Aug 14, 2026 · Updated 2 times
Summary
This trial asks whether injecting dexamethasone, a steroid, before a root canal can reduce pain afterward. Adults with a painful, inflamed tooth will receive the injection either in the cheek or near the tooth, or just standard numbing. Pain levels will be tracked for three days to see if the steroid helps.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- dexamethasone
- What this could lead to
- If effective, this could offer a simple, low-cost way to reduce pain after root canal treatment, potentially decreasing the need for painkillers.
- What could go wrong
- This is a small, early-stage trial, and results may not apply to all patients. Dexamethasone injections can cause local side effects like pain or swelling, and the benefit over standard care is not yet proven.
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
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
66 people
The number who actually took part.
- Started
-
Mar 2024
- Finished
-
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 60 years
- Sex
-
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: * Both genders * Older than age of (18 to 60) years * Participants willing to commit for the entire period of the trial and agreed to sign the written consent after full explanation of the study * Having a mandibular molar tooth with vital pulp * These patients were also suffering from symptomatic irreversible pulpitis ,intermittent or continuous sharp pain that lasts longer after removal of the stimulus * Patients with moderate to severe symptoms VAS≥4 Exclusion Criteria: * Vulnerable group; pregnant females, mentally ill and diseased patientsetc.… * Patients irritable to local anesthesia * Patients who are supposed to take plain anesthesia * Use of analgesic or antibiotic within 6 hours before the visit * Absence of bleeding in the pulp chamber during cavity preparation * Severe periodontal disease b- Patients' randomization, allocation and blinding:
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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
-
Faculty of Dentistry Ain Shams University
Cairo, Egypt
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