Which nerve block eases chest surgery pain better?
NCT ID NCT07799844
First seen Sep 02, 2026 · Last updated Sep 03, 2026 · Updated 1 time
Summary
This trial tests two ultrasound-guided nerve blocks for pain relief after thoracotomy, a surgery that opens the chest. One block targets the paravertebral space, while the other targets a point between the transverse process and the pleura. Researchers will compare how much morphine patients need in the first 24 hours after surgery, along with pain scores and complications. The study includes adults aged 18 to 65 scheduled for elective thoracotomy.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- levobupivacaine
- What this could lead to
- If one block proves better, it could offer safer and more effective pain control after chest surgery, reducing the need for morphine.
- What could go wrong
- This is a small, early-stage trial, so results may not apply to all patients. Both blocks carry risks like accidental lung puncture or local anesthetic side effects.
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
-
60 people
The number who actually took part.
- Started
-
Jan 2024
- Finished
-
Sep 2024
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients aged from 18 to 65 years old * both sexes, American Society of Anesthesiologists (ASA) classification I \& II * scheduled for elective thoracotomy. Exclusion Criteria: Patient refusal. · BMI ≥ 35. * Bleeding diathesis. * Patients with local anesthetic allergy. * Neurological disease. * Infections at the needle site.
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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.
Contacts and locations
Locations
-
Tanta University
Tanta, Egypt
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