Could a new needle design make dental shots Pain-Free?
NCT ID NCT07703410
First seen Jul 14, 2026 · Last updated Jul 15, 2026 · Updated 1 time
Summary
This trial compares a specially designed needle tip, the Transcodent painless needle, with a standard dental needle to see if it causes less pain during injections in the upper front teeth area. Sixty adults needing dental work on both sides of their mouth will receive injections with both needle types, and they will rate their pain right after each injection. The goal is to find a way to make dental procedures more comfortable for patients.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a dental needle tip with a three-edge lancet grinding bevel and silicone coating designed to reduce injection pain
- What this could lead to
- If effective, this needle tip could make dental injections less painful, improving patient comfort during routine procedures.
- What could go wrong
- This is a small, early-stage trial with only 60 participants, so results may not apply to everyone. The needle tip may not significantly reduce pain compared to standard needles.
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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Jun 2026
An estimate. Start dates often move.
- Expected to finish
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Jul 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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18 to 60 years
- Sex
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Anyone
- Healthy volunteers
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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: Adults aged 18 to 60 years. Patients requiring bilateral maxillary anterior infiltration anesthesia for dental treatment. Patients undergoing endodontic procedures involving maxillary canines or premolars. Presence of healthy maxillary teeth on both sides suitable for infiltration anesthesia. Individuals with no systemic disease or neurological disorder affecting pain perception. Ability to understand the study procedures and provide written informed consent. Both male and female participants. Exclusion Criteria: Pregnant or lactating women. Use of analgesics, sedatives, or other pain-modifying medications within the previous 12 hours. Known allergy or hypersensitivity to local anesthetics, benzocaine, lidocaine, or epinephrine. Presence of active infection, inflammation, swelling, or pathology at the injection site. Severe dental anxiety, needle phobia, or inability to cooperate with study procedures. Individuals unable or unwilling to provide informed consent.
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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
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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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