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Tummy tuck pain relief: nerve block may cut opioid use

NCT ID NCT01604694

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 This study
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 Results may not be published yet.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
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This status has not been confirmed recently, so it may be out of date.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 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tested whether an ultrasound-guided nerve block (TAP block) using the anesthetic levobupivacaine could reduce pain and the need for opioid painkillers after abdominoplasty (tummy tuck). Fifty-two adults undergoing the surgery were randomly assigned to receive either the active nerve block or a placebo (saline) injection. The main goal was to measure opioid use in the first 24 hours after surgery.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
levobupivacaine (a local anesthetic) given as a TAP block injection
What this could lead to
If effective, this could provide a standard way to reduce pain and opioid use after tummy tuck surgery.
What could go wrong
This is a small, single-center trial with only 52 participants, so results may not apply broadly. The benefit over placebo may be modest.

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

52 people

The number who actually took part.

Start date

Jun 2012

Finished

Oct 2013

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: * ASA1 or 2 patients * Undergoing abdominoplasty surgery in Centre François Xavier Michelet at Bordeaux University hospital * Age \>18 years old * Patient agreement by signing an informed consent Exclusion Criteria: * Psychiatric or neurological disease * Contraindication to regional anesthesia (haemostatic disorders, infection near to insertion point) * Double surgery * Long term opioid therapy * Pregnancy or breast-feeding * Allergy to any drug used in anesthesic or surgical procedure

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Conditions

The condition(s) this trial relates to.

Bites and Stings

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • CHU de Bordeaux, Centre François-Xavier Michelet

    Bordeaux, 33076, France

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Other studies related to the condition(s) this trial covers.