Simple nerve block could prevent Post-Surgery heart rhythm problems
NCT ID NCT05932485
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether a stellate ganglion block (a nerve injection) before coronary artery bypass surgery can prevent new atrial fibrillation, a common complication. 108 patients were included. The approach aims to calm the nervous system and reduce inflammation. Results could lead to a simple way to lower stroke and heart failure risks after surgery.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- stellate ganglion block with ropivacaine
- What this could lead to
- If it works, this could offer a simple procedure to lower the risk of atrial fibrillation after heart bypass surgery, reducing stroke and other complications.
- What could go wrong
- This is a small, single-center study with 108 patients. The nerve block may not work for everyone, and there are risks like bleeding or nerve damage from the injection.
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
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108 people
The number who actually took part.
- Started
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Jun 2023
- Finished
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Jun 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
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18 to 80 years
- 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.
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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 undergoing first-time and elective coronary artery bypass grafting; * ASA grade II-IV; * The preoperative ECG showed sinus heart rate. Exclusion Criteria: * The patient refused to participate in this study; * Surgical procedures include any other type of heart surgery in addition to CABG; * Allergic to known general anesthesia drugs; * Patients with a history of neck surgery or abnormal neck anatomy; * Patients with contraindications to SGB.
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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
-
the Affiliated Hospital of Yangzhou University, Yangzhou University
Yangzhou, Jiangsu, China
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- A soft patch that watches your heart beat in real time
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