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Recruiting NCT06271707

Stellate Ganglion Block

Conditions: Esophagectomy, Pneumonectomy, Lobectomy

Sex: All
Ages: 18 Years – 85 Years
Healthy volunteers: No
Phase: PHASE4
Enrollment: 48
Sponsor: University of Minnesota

Location: University of Minnesota Minneapolis Minnesota

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.

Eligibility Criteria

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

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT06271707). StuddyBuddy aggregates publicly available trial information.