ClinicalTrials.Veeva

Menu

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

A

Air Force Military Medical University of People's Liberation Army

Status

Enrolling

Conditions

Adult Patients Undergoing CABG

Treatments

Procedure: Stellate Ganglion Block

Study type

Interventional

Funder types

Other

Identifiers

NCT07271615
KY20250716

Details and patient eligibility

About

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.

Enrollment

60 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

  • History of prior cardiac surgery or atrial fibrillation ablation;
  • Emergency coronary artery bypass grafting (CABG);
  • Concomitant cardiac procedures (e.g., congenital heart disease repair, left ventricular reconstruction, valve surgery, or aortic surgery);
  • Critical preoperative status requiring mechanical or pharmacological support before CABG;
  • Left ventricular ejection fraction (LVEF) <35%;
  • 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%);
  • Severe left atrial enlargement (left atrial anteroposterior diameter >55 mm);
  • Poorly controlled hyperthyroidism;
  • Conditions requiring radiotherapy, chemotherapy, or long-term hormonal therapy;
  • Patients with known clinical contraindications to stellate ganglion block (SGB).

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

60 participants in 2 patient groups

Control group(C group)
No Intervention group
Description:
the best available treatment without block (usual care)
Stellate Ganglion Block(S group)
Other group
Description:
Ultrasound-guided stellate ganglion block with ropivacaine
Treatment:
Procedure: Stellate Ganglion Block

Trial contacts and locations

1

Loading...

Central trial contact

Chong Lei

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems