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NCT07271615Completed

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

Source: ClinicalTrials.gov · Last updated 4 Aug 2026

Brief summary (registry, in English)

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.

Status (registry)
Completed
Study type
Interventional
Enrollment
60 (actual)
First submitted
26 Nov 2025
Start date
19 Nov 2025
Primary completion date
31 May 2026
Lead sponsor
Xijing Hospital
NCT number
NCT07271615

What you commit to

  • Study type: Interventional
  • Participants enrolled: 60
  • From 19 Nov 2025 to the primary completion date, 31 May 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • History of prior cardiac surgery or atrial fibrillation ablation;
  • Concomitant cardiac procedures (e.g., congenital heart disease repair, left ventricular reconstruction, valve surgery, or aortic surgery);

Other illness

  • History of atrial fibrillation (defined as a supraventricular tachyarrhythmia characterized by rapid and irregular atrial electrical activity);
  • Significant mitral valve disease (mitral valve area \<1.5 cm² or regurgitant jet area \<4 cm²), significant aortic valve disease (valve area \<1.5 cm² or regurgitant jet-to-left ventricular outflow tract ratio \>25%);
  • Conditions requiring radiotherapy, chemotherapy, or long-term hormonal therapy;

Lab values

  • Left ventricular ejection fraction (LVEF) \<35%;

Other

  • Emergency coronary artery bypass grafting (CABG);
  • Critical preoperative status requiring mechanical or pharmacological support before CABG;
  • Severe left atrial enlargement (left atrial anteroposterior diameter \>55 mm);
  • Poorly controlled hyperthyroidism;
  • Patients with known clinical contraindications to stellate ganglion block (SGB).

Who the study is looking for

  • more than 18 years old
  • undergoing CABG
  • Provide informed consent

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Xijing hospital
Coordinator of this site? Confirm its status
Xi'anChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.