Pain relief without opioids? lidocaine dosing trial for bariatric surgery
NCT ID NCT03095404
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study was designed to find the best dose of intravenous lidocaine for controlling pain after bariatric bowel surgery. Lidocaine is a local anesthetic that may reduce the need for opioids, which can cause nausea and other side effects. The trial planned to compare two doses in adults undergoing major bowel surgery, but it was withdrawn before any participants were enrolled.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- lidocaine
- What this could lead to
- If successful, this could point toward a standard lidocaine dosing schedule to improve pain relief and reduce opioid use after bariatric surgery.
- What could go wrong
- This trial was withdrawn before enrolling any participants, so no data exists. The findings may not apply to other surgeries or patient groups.
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
-
Early phase 1
The earliest testing in people: a first look at safety, in a very small group.
- Started
-
Oct 2022
- Finished
-
Aug 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 years and older
- 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: * Bariatric patients 18 years or older undergoing major bowel surgery * Patient capable to complete informed consent Exclusion Criteria: * Pediatric population * Inability to complete informed consent * Patient refusal * Chronic aspirin or NSAID intake * Known allergy to aspirin and/or NSAIDs, or lidocaine * History of bronchial asthma requiring intubation * Peptic ulceration * Coagulopathy * Renal insufficiency * Opioid abuse * Pregnancy * Conversion from laparoscopic to open surgery. * Other relative contraindications for lidocaine; unstable CAD, Recent MI, Heart Failure, Heart Block, Electrolyte Disturbances, Liver Disease, Cardiac Dysrhythmias, and Seizure Disorders.
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
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