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Pain relief without opioids? lidocaine dosing trial for bariatric surgery

NCT ID NCT03095404

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled This study
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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 The trial planned to compare two doses in adults undergoing major bowel surgery, but it was withdrawn before any participants were enrolled.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This trial was withdrawn before enrolling any participants, so no data exists.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

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

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