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Paravertebral Block to Reduce the Incidence of New Onset Atrial Fibrillation After Cardiac Surgery

Anesthesia, Local Clinical Trial

Official title:
Paravertebral Block to Reduce the Incidence of New Onset Atrial Fibrillation After Cardiac Surgery: A Prospective Randomized Controlled Pilot Trial

Clinical Trial Summary

The purpose if this pilot study is to determine if a perioperative infusion of 0.2% ropivacaine via bilateral T3 paravertebral catheters can decrease the incidence of new onset atrial fibrillation following primary CABG and/or valve surgery and compare a number of secondary outcomes.

Clinical Trial Description

Patients in the intervention group will have ultrasound guided bilateral T3 paravertebral catheters placed prior to surgery. Prior to surgery, these patients will have 5ml of 1.5% lidocaine with 1:200,000 epinephrine injected in each catheter. Ropivacaine 0.2% will be administered via programmed intermittent bolus of 7ml every 60 minutes through each catheter during and after surgery. Patients in the control group will receive no block and undergo surgery with routine anesthetic care guided by their cardiac anesthesiologist. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04472299
Study type Interventional
Source University of Minnesota
Contact Candace Nelson
Phone 612-626-2465
Email nelso377@umn.edu
Status Recruiting
Phase Phase 4
Start date April 9, 2021
Completion date July 1, 2024
View Details
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