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Battle of the pain blocks: ultrasound vs. Video-Guided in lung surgery

NCT ID NCT04579276

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 compares two methods of giving a nerve block to control pain after lung surgery (thoracotomy). One method uses ultrasound to guide the needle, the other uses a camera inside the chest during minimally invasive surgery. The goal is to see which approach reduces the need for morphine and improves recovery. 180 adults having lung surgery will take part.

What this could mean

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

Active substance
Thoracic paravertebral block (pain relief procedure)
What this could lead to
If successful, this could show that one method of pain block is better or easier, leading to less morphine use and faster recovery after lung surgery.
What could go wrong
This is a small, single-center study comparing two established techniques, so any difference may not apply to all hospitals or patients. The main risk is that neither method proves clearly superior.

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

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

180 people

The number who actually took part.

Started

Sep 2020

Finished

Dec 2021

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: * Male or female ≥ 18 years of age. * VATS or RATS with lung resection including wedges, segmentectomies or lobectomies. * Signed consent. * Scheduled surgeries. Exclusion Criteria: * Patient refusing to sign the consent form. * Minors. * Patients under any guardianship. * All surgeries with pleura intervention: talc, pleurectomy, wall resection. * Non trained anesthesiologist to ultrasound TPB. * Presence of pain or daily use of painkillers prior to surgery. * Medical history of homolateral thoracic surgery.

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As listed by the trial registrant

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

Contacts and locations

Locations

  • assistance publique hôpitaux de Marseille

    Marseille, 13354, France

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