Jaw surgery pain study: which numbing drug works best?
NCT ID NCT06450028
First seen Jun 25, 2026 · Last updated Aug 05, 2026 · Updated 6 times
Summary
This study compared two common numbing drugs, lidocaine and bupivacaine, in 60 people aged 15–35 having jaw surgery. Researchers measured pain, numbness, and touch sensation after surgery. The goal is to find which drug gives patients a better recovery experience.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- lidocaine and bupivacaine (local anesthetics)
- What this could lead to
- If this study shows one drug works better, surgeons may use it to reduce pain and numbness after jaw surgery.
- What could go wrong
- This is a small, completed Phase 4 trial with only 60 participants. Results may not apply to everyone, and both drugs are already standard care, so no major breakthrough is expected.
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
-
64 people
The number who actually took part.
- Started
-
Oct 2024
- Finished
-
Nov 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
-
15 to 35 years
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Undergoing an orthognathic procedure at Boston Children's Hospital * Between the ages of 15 and 35 years old Exclusion Criteria: * Any patient undergoing any other procedures in addition to their orthognathic procedure during the same sedation period (extraction, bone graft, etc.). * Any patient with a history of chronic pain. * Any patient with a history of an allergic reaction to bupivacaine or lidocaine. * Any patient with known neurologic changes to the lip or chin. * Any patient not enrolled in an Enhanced Recovery After Surgery (ERAS) Protocol. * Any patient known to be pregnant or with a positive pregnancy test prior to the procedure.
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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
-
Boston Children's Hospital
Boston, Massachusetts, 02115, United States
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