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NCT06271707 Clinical Trial

Stellate Ganglion Block

Esophagectomy Clinical Trial

Official title:
Left Sided Stellate Ganglion Blocks Impact on the Rate of Post-operative Atrial Fibrillation in Patients Undergoing Thoracic Surgery: A Pilot Study

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT06271707
Other study ID # ANES-2024-32720
Secondary ID
Status Not yet recruiting
Phase Phase 4
First received
Last updated
Start date July 1, 2024
Est. completion date September 30, 2026

Study information
Verified date April 2024
Source University of Minnesota
Contact Candace Nelson
Email nelso377@umn.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine if the addition of an ultrasound guided left sided stellate ganglion block with bupivacaine in patients undergoing esophagectomy, pneumonectomy, or lobectomy will result in lower rates of postoperative atrial fibrillation as compared to standard of care.

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 48
Est. completion date September 30, 2026
Est. primary completion date June 30, 2026
Accepts healthy volunteers No
Gender All
Age group 18 Years to 85 Years
Eligibility Inclusion Criteria: - Patients undergoing esophagectomy, pneumonectomy, or lobectomy aged 18-85. Exclusion Criteria: - Patients who have an exclusion to regional anesthesia. - Patients who have exclusion to stellate blockade. - Patients who are pregnant assessed via self-report or pregnancy test if they have taken one

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• 0.5% bupivacaine
an ultrasound guided left stellate ganglion block with 5 mL of 0.5% bupivacaine
Other:
• Saline
an ultrasound guided left stellate ganglion block with 5 mL of saline

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
University of Minnesota

Outcome
Type Measure Description Time frame Safety issue
Primary an ultrasound guided left stellate ganglion block with 5 mL of saline. Incidence of Atrial fibrillation in the first 168 hours after surgery. 168 hours after surgery
Primary Atrial fibrillation; Other arrhythmias; Adverse events. Atrial fibrillation in first 24, 48, 72, 96, 120, and 144 hours; Other arrhythmias in first 24, 48, 72, 96, 120, 144 and 168 hours; Adverse events. 168 hours after surgery
See also
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