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Trial Title:
Stellate Ganglion Block
NCT ID:
NCT06271707
Condition:
Esophagectomy
Pneumonectomy
Lobectomy
Conditions: Official terms:
Ganglion Cysts
Bupivacaine
Conditions: Keywords:
Esophagectomy
Pneumonectomy
Lobectomy
Stellate Ganglion Block
Study type:
Interventional
Study phase:
Phase 4
Overall status:
Not yet recruiting
Study design:
Allocation:
Randomized
Intervention model:
Parallel Assignment
Primary purpose:
Prevention
Masking:
Triple (Participant, Investigator, Outcomes Assessor)
Masking description:
This is a double blind randomized prospective controlled trial. Randomization will be
1:1.
Intervention:
Intervention type:
Drug
Intervention name:
0.5% bupivacaine
Description:
an ultrasound guided left stellate ganglion block with 5 mL of 0.5% bupivacaine
Arm group label:
Group 1
Intervention type:
Other
Intervention name:
Saline
Description:
an ultrasound guided left stellate ganglion block with 5 mL of saline
Arm group label:
Group 2
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.
Criteria for 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
Gender:
All
Minimum age:
18 Years
Maximum age:
85 Years
Healthy volunteers:
No
Start date:
December 15, 2024
Completion date:
February 15, 2027
Lead sponsor:
Agency:
University of Minnesota
Agency class:
Other
Source:
University of Minnesota
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT06271707
