Chill out tooth pain: cooling inside of tooth during root canal may ease ache
NCT ID NCT07710833
First seen Jul 17, 2026 · Last updated Jul 17, 2026
Summary
This study tests whether using cooled liquid to clean the inside of a tooth during root canal treatment can reduce pain afterward. It includes adults with certain tooth conditions who need a root canal. The approach involves comparing cooled versus room-temperature irrigation to see which leads to less discomfort.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- cooled sodium hypochlorite (NaOCl) irrigation during root canal treatment
- What this could lead to
- If effective, this simple cooling technique could become a standard way to reduce pain after root canal treatment.
- What could go wrong
- This is a small, early-stage trial, so results may not apply to all patients or tooth types. The cooling effect on pain may be minimal or no better than room-temperature irrigation.
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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
-
132 people
The number who actually took part.
- Started
-
May 2026
- Finished
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Jul 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 70 years
- Sex
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Anyone
- Healthy volunteers
-
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: 1. Systemically healthy patients with 18-70 years of age 2. Single-rooted teeth with a single root canal, diagnosed with either AIP and normal periapical tissues or AAP. Pulpal and periapical diagnoses were established according to the American Association of Endodontists (AAE) \[20\] diagnostic terminology. Included teeth were categorized into 2 diagnostic groups: AIP with normal periapical tissues and AAP associated with pulp necrosis. AIP was provisionally diagnosed in teeth with extremely deep caries approximating or reaching the pulp, a positive response to cold testing (Dispodent, Nadu, India), and no clinical symptoms. Periapical radiographs showed a PAI score of 1 without periodontal ligament widening. The diagnosis was confirmed intraoperatively by persistent pulpal bleeding that remained uncontrolled after 10 minutes of application of a sterile cotton pellet moistened with 2.5% sodium hypochlorite. AAP was diagnosed in teeth with a PAI score of ≥3 in the absence of clinical symptoms. None of the included teeth exhibited tenderness to percussion. All periapical radiographs were obtained using a phosphor storage plate system and the paralleling technique (Myray parallel holder, NDental, Imola, Italy) under standardized exposure parameters (70 kV, 8 mA, 0.360 s). Exclusion Criteria: 1) Teeth with canal calcification, complex or atypical canal anatomy, root resorption, incomplete root development, or a history of endodontic treatment of the study tooth. 2\) Teeth initially diagnosed with AIP in which pulpal bleeding was controlled within 10 min after access cavity preparation, as these teeth were considered eligible for vital pulp therapy. 3\) Teeth initially diagnosed with AIP in which pulp necrosis was identified after access cavity preparation. 4\) Teeth in which root canal treatment could not be completed in a single visit. 5\) Patients who had taken analgesics within 12 hours before the appointment or antibiotics within the previous month. 6\) Teeth with periodontal probing depths \>3 mm or clinical/radiographic signs of periodontal disease. 7\) Teeth with insufficient coronal tooth structure to allow an adequate ferrule. 8\) Pregnant or breastfeeding patients and patients with systemic conditions or regular medication use that could affect treatment outcomes.
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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
-
Recep Tayyip Erdoğan University Faculty of Dentistry, Department of Endodontics
Rize, Centre, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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