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New study aims to improve pain control after lung surgery

NCT ID NCT01082744

Symptom relief Sponsor: Hospices Civils de Lyon Source: ClinicalTrials.gov ↗

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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

Summary

This study tested two different drug combinations given through a small tube near the spine to control pain after video-assisted lung surgery. 90 adults participated to see if adding sufentanil to ropivacaine reduces the need for morphine and improves pain scores compared to ropivacaine alone. The goal is to find the best way to manage pain after this type of surgery.

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 3

Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.

Participants

90 people

The number who actually took part.

Start date

Mar 2010

Finished

Dec 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 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: * Patient scheduled for planned video-assisted thoracic surgery * Patient that consent to participate * Planned placement of paravertebral catheter * Patient having a medical insurance Exclusion Criteria: * Patient less than 18 years * Refusal to participate * Known pregnancy * Known allergies to local anesthetics, sufentanil and /or to iodinated contrast material * Intolerance to sufentanil and/or morphine * Chronic consumption of opiates * Preoperative chronic pain syndrome * Patient having a contraindication to placement of paravertebrtal catheter

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Conditions

The condition(s) this trial relates to.

Chronic Pain Pain, Postoperative

As listed by the trial registrant

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

Pain, postoperative

Contacts and locations

Locations

  • Hospices Civils de Lyon, Hopital Louis Pradel, Department of Anesthesiology

    Bron, 69500, France

More trials for these conditions

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