RecruitingNot ApplicableNCT07271615

Effect of Preoperative Stellate Ganglion Block on Postoperative Atrial Fibrillation After Coronary Artery Bypass Grafting

Preoperative Stellate Ganglion Block Reduce the Incidence of Postoperative Atrial Fibrillation After Coronary Artery Bypass Grafting: A Prospective, Randomized Controlled Pilot Trial


Sponsor

Xijing Hospital

Enrollment

60 participants

Start Date

Nov 19, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The primary objective of this study is to determine the feasibility of preoperative stellate ganglion block in reducing the incidence of postoperative atrial fibrillation in patients undergoing CABG.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing whether a nerve block given before coronary artery bypass grafting (open-heart bypass surgery) can reduce the risk of developing an irregular heartbeat called atrial fibrillation after the surgery. The nerve block temporarily numbs the stellate ganglion, a cluster of nerves in the neck that influences heart rhythm. **You may be eligible if...** - You are over 18 years old - You are scheduled for planned (non-emergency) bypass heart surgery (CABG) - You are able to give informed consent **You may NOT be eligible if...** - You have had prior heart surgery or a prior ablation for atrial fibrillation - You are having emergency bypass surgery - You are having additional heart procedures at the same time (e.g., valve repair, aortic surgery) - You have critical preoperative conditions or severe instability Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

PROCEDUREStellate Ganglion Block

Ultrasound-guided stellate ganglion block with ropivacaine


Locations(1)

Xijing Hospital

Xi'an, Shaanxi, China

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NCT07271615