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New nerve block could ease pain during 'Awake' lung surgery

NCT ID NCT07440199

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study compares two types of nerve blocks for pain control during a type of lung surgery that does not require a breathing tube. The goal is to see if a newer block (serratus posterior superior intercostal plane block) works as well as or better than a commonly used block (serratus anterior plane block) for reducing pain and the need for anesthesia during and after surgery. The trial will involve 70 adults undergoing non-intubated, single-port video-assisted thoracoscopic surgery.

What this could mean

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

Active substance
nerve block (serratus posterior superior intercostal plane block or serratus anterior plane block)
What this could lead to
If successful, this could identify a better nerve block technique for pain control during minimally invasive lung surgery, potentially improving recovery and reducing complications.
What could go wrong
This is a small, early-phase study (70 participants) comparing two similar techniques. Results may not apply to all patients or surgeries, and the newer block may not prove 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

About 70 people

The number the study aims to enrol. It can still change while the study runs.

Started

Jan 2026

Expected to finish

Aug 2026

An estimate. End dates often move.

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: The study included patients who: * were aged 18-65 years, * had an American Society of Anaesthesiologists (ASA) physical status classification of I-III, * had a body mass index (BMI) \< 35 kg/m², * read and signed the informed consent form. Exclusion Criteria: Patients; * Unable to communicate in Turkish or refusing to participate in the study, * Unable to use the numerical pain rating scale (NRS), * History of allergy to local anaesthetics or analgesics used in the study, * Pregnant or breastfeeding, * History of uncontrolled anxiety disorder or substance dependence, * Previous thoracic surgery or history of thoracic trauma, * Widespread pleural adhesions detected during preoperative assessment, * Neuromuscular or peripheral nervous system disease, * Diabetes mellitus, hepatic or renal insufficiency, or coagulation disorder, * Chronic opioid or steroid use, * Widespread pain syndrome, * Receiving anticoagulant therapy, * Patients with infection detected in the area where the block will be applied were excluded.

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Sign up to get updates when this study changes or when new studies for This study evaluates the effects of different fascial plane blocks on intraoperative anesthesia and analgesic consumption in non-intubated vats procedures are added.

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As listed by the trial registrant

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

How to take part

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  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

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Contacts and locations

Locations

  • Fırat University Faculty of Medicine Hospital

    RECRUITING

    Elâzığ, 23100, Turkey (Türkiye)