Tiny particles, big relief? Nano-Calcium hydroxide may soothe root canal pain
NCT ID NCT07057336
First seen Aug 31, 2026 · Last updated Sep 01, 2026 · Updated 1 time
Summary
This trial tests whether a nano-sized form of calcium hydroxide, placed inside the tooth after cleaning, reduces pain following root canal treatment compared to the conventional version. Adults aged 18 to 65 with a dead nerve in a single-rooted tooth and an infection at the tip of the root are eligible. Participants receive either conventional or nano-calcium hydroxide as a temporary filling, then rate their pain on a standard scale. The goal is to see if the nano version offers better pain control during recovery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- nano-sized calcium hydroxide
- What this could lead to
- If it works, nano-calcium hydroxide could become a standard intracanal medicament that makes root canal recovery more comfortable.
- What could go wrong
- This is a small, early-stage trial, and the benefit may be modest or not clearly better than the conventional treatment. Pain after root canal varies widely among individuals.
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
-
90 people
The number who actually took part.
- Started
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May 2024
- Finished
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Dec 2025
- 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
-
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: * Patients aged 18-65 years * Single-rooted permanent maxillary or mandibular teeth * Asymptomatic teeth with necrotic pulps confirmed by negative response to cold test * Presence of periapical radiolucency (PAI score 2-5) * No sensitivity to percussion or palpation * Patients who signed informed consent Exclusion Criteria: * Pregnancy or lactation * Systemic diseases requiring antibiotic prophylaxis (e.g., infective endocarditis, immunosuppression) * Use of antibiotics, corticosteroids, or analgesics within the past 7 days * History of chemotherapy or radiotherapy * Uncontrolled diabetes mellitus or hypertension * Chronic renal failure, hematologic disorders * Teeth with root resorption, previous endodontic treatment, or multirooted anatomy * Teeth with periodontal pockets \>4 mm or mobility * Inability to attend follow-up visits * Patients with extensive coronal destruction rendering definitive restoration unfeasible
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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
-
Cukurova University
Adana, Sarıçam, 01250, Turkey (Türkiye)
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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