Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Which numbing drug works best for leg surgery?

NCT ID NCT01935596

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study compared two numbing medicines, levobupivacaine and ropivacaine, given as spinal anesthesia for leg surgery. Fifty adults with leg injuries took part. Researchers measured how long numbness and muscle relaxation lasted. The goal was to see if one drug works better or lasts longer than the other.

What this could mean

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

Active substance
levobupivacaine and ropivacaine (local anesthetics)
What this could lead to
If one anesthetic works better, it could help doctors choose the best option for numbing during leg surgery, improving patient comfort and recovery.
What could go wrong
This is a small, completed study with only 50 people, so results may not apply to everyone. Both drugs are already approved, 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

50 people

The number who actually took part.

Start date

May 2013

Finished

Apr 2014

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 to 65 years

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: * patient admitted to the emergency for lower limb trauma, * age over 18 years and below 65 years * lower limb trauma surgery can be performed under spinal anesthesia. Exclusion Criteria: * Refusal of patients to participate in the study, * Patient with cons-indication to spinal anesthesia: * Local anesthetic allergy agents (1/13000) * bleeding disorders, including pharmacological origin * infection at the puncture site, * refusal of spinal anesthesia by the patient, * Patient trust, * Patients whose coagulation is abnormal. * Patients with cognitive impairment or incapacitated adult, * Multiple trauma, * Porphyria, * Central preexisting neuropathy, * A history of spinal surgery, * Epilepsy uncontrolled by treatment, * Hypovolemia, * Pregnant or lactating women, * Participation in another ongoing clinical trial, * Patient on anticoagulant therapy, * Patient not affiliated with a social security system.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Patients undergoing lower limb surgery are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

As listed by the trial registrant

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

Contacts and locations

Locations

  • Hervé DUPONT

    Amiens, Picardie, 80054, France