Nerve blocks may help heart surgery patients breathe easier after operation
NCT ID NCT05958823
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether two types of nerve blocks (SAP and PECS) can reduce pain and shorten the time patients need a breathing tube after heart bypass surgery. 243 adults undergoing open heart surgery received either a nerve block or standard pain medication. Researchers measured pain scores, opioid use, and recovery times to see which approach works best.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- nerve blocks (serratus anterior plane block and pectoral nerve blocks I-II)
- What this could lead to
- If effective, these nerve blocks could become a standard way to reduce pain and speed recovery after heart surgery.
- What could go wrong
- This is a completed trial, but results are not yet published. Nerve blocks carry small risks like bleeding or infection, and may not work better than standard painkillers.
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
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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
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243 people
The number who actually took part.
- Started
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Jun 2023
- Finished
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Nov 2024
- 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.
- Ages
-
20 to 65 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: * Agreeing to participate in the study, * 20-65 years old * ASA I-II-III * Open heart surgery Exclusion Criteria: * Refusal to participate in the study * 20 years old, over 65 years old * Pregnancy * Presence of bleeding diathesis * Liver or kidney failure * Receiving effective treatment on immunity * Immune suppressed * Those with BMI ≥30
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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
-
Van Yuzuncu Yil University
Van, Turkey, 65100, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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