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

Gå till den engelska sidan

Cure My Disease

Don't miss your cure!

 Log in / Sign up

New study tests better pain relief for lung surgery patients

NCT ID NCT06289790

Symptom relief Sponsor: Central Clinical Hospital of the Ministry of Internal Affairs and Administration, Warsaw, Poland 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 looked at 61 adults having lung surgery to see which pain relief method works better: a nerve block (ESP block) or medicine given through a vein (IV lignocaine). The main goals were to measure pain levels and how much extra pain medicine patients needed after surgery. The results help doctors choose the best way to keep patients comfortable.

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

61 people

The number who actually took part.

Started

Apr 2024

Finished

Oct 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: * Age \>18 * VATS for tumor resection or partial lung resection in emphysema * Written, informed consent obtained 1 day prior to surgery Exclusion criteria: * Lack of consent for ESP blockade * History of allergy to local anaesthetics * Other contraindications to ESP blockade * American Society of Anesthesiologists(ASA) Physical Status Classification value 4 or higher * VATS for indications other than tumor resection or partial lung resection in emphysema * Insulin- dependent diabetes mellitus * More than 1 chest drain post-operatively * Conversion to thoracotomy * Chronic opioid use prior to surgery defined as opioid administration for at least 3 months during the last 12 months * History of alcohol abuse * Suspected technical difficulties with performing the ESP block (e.g. obesity) * Inadequate spread of the local anaesthetic during the ESP block * Cognitive impairment that might cause an inaccurate assessment of pain levels

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Thoracic surgery, video assisted 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.

Thoracic surgery, video assisted

Contacts and locations

Locations

  • National Medical Institute of the Ministry of the Interior and Administration

    Warsaw, Masovian Voivodeship, 02-507, Poland

More trials for these conditions

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