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Spinal shot may boost recovery after lung surgery

NCT ID NCT07231926

Symptom relief Sponsor: Ataturk University 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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Sep 04, 2026 · Updated 2 times

Summary

This study looks at whether adding a spinal morphine injection to standard pain control (nerve block and sedation) helps people recover better after video-assisted lung surgery. About 52 adults having planned lung surgery will be randomly assigned to receive either the extra spinal morphine or not. The main goal is to see if the combination improves overall recovery and reduces inflammation.

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

64 people

The number who actually took part.

Started

Dec 2025

Finished

Jul 2026

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 70 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: * Elective video-assisted thoracoscopic surgery (VATS) planned * Age 18-70 years * ASA physical status I-III * Body mass index (BMI) \<35 kg/m² Exclusion Criteria: * Coagulopathy * Opioid dependence or intolerance * Allergy to local anesthetics * Contraindications to neuraxial blockade * Chronic pain history * Renal or hepatic failure

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As listed by the trial registrant

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

Postoperative pain management in video-assisted thoracoscopic surgery

Contacts and locations

Locations

  • Ataturk University

    Erzurum, 25000, Turkey (Türkiye)

  • Ataturk University

    Erzurum, 25240, Turkey (Türkiye)