Chest surgery pain study seeks best relief strategy
NCT ID NCT07694141
First seen Jul 09, 2026 · Last updated Jul 21, 2026 · Updated 3 times
Summary
This study observes pain control in adults undergoing planned chest surgery. It compares standard epidural analgesia with a newer nerve block technique called erector spinae plane block, which is safer to place. Researchers will track pain scores and complications to see which method leads to better recovery. The goal is to improve pain management for future patients.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this study could help identify which pain management technique works best for thoracic surgery patients, potentially improving recovery and reducing complications.
- What could go wrong
- This is an observational study, not a controlled trial, so it cannot prove cause and effect. Results may be influenced by patient differences or standard practice variations.
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.
- Participants
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About 160 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Nov 2025
- Expected to finish
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Jan 2027
An estimate. End dates often move.
- Lead sponsor
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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.
Who is studied
The study will include ASA I-III patients scheduled for thoracic surgery at the Doctor Negrín University Hospital of Gran Canaria
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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: * Patients undergoing thoracic surgery between July 1 and October 31, 2020. * Age over 18. * ASA I-III. * Signed informed consent Exclusion Criteria: * ASA IV-V. * Chronic opioid treatment or treatment in the Chronic Pain Unit. * Intravenous drug abuse. * Local anesthetic allergy. * Language barrier, cognitive impairment, or inability to participate in clinical assessment during the study. * BMI \<18 or \>35 kg/m2
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Hospital Universitario de Gran Canaria Doctor Negrín
RECRUITINGLas Palmas de Gran Canaria, Las Palmas, 35002, Spain
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Other studies related to the condition(s) this trial covers.
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