Clinical Trials Directory

Trials / Unknown

UnknownNCT03781440

Regional Anesthesia for Cardiothoracic Enhanced Recovery

Regional Anesthesia for Cardiothoracic Enhanced Recovery for Patients Undergoing Cardiac Surgery Via Sternotomy

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Stanford University · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The erector spinae plane block (ESPB) is a novel regional analgesic technique that provides pain relief with a peripheral nerve block catheter. The goal of this study is to see if bilateral ESPB catheters can improve clinical outcomes in patients undergoing cardiac surgery via sternotomy, such as decreasing the duration of postoperative mechanical ventilation, need for intravenous opioid medications, length of stay in the intensive care unit (ICU), and improving pain scores.

Conditions

Interventions

TypeNameDescription
PROCEDUREBilateral ESP catheter with lidocaineAll participants will get the Erector Spinae Plane (ESP) catheters. Prior to transfer to the operating room, participants will receive bilateral ESP catheters at T7 level under ultrasound guidance. This arm is the treatment group and will receive lidocaine via alternating side automated infusion pump bolus dosing, continued until chest tube removal or postoperative day 5 (whichever occurs earliest).
PROCEDUREBilateral ESP catheter with salineAll participants will get the Erector Spinae Plane (ESP) catheters. This arm is the control group and will have normal saline administered via ESP catheters, continued until chest tube removal or postoperative day 5 (whichever occurs earliest).

Timeline

Start date
2020-01-01
Primary completion
2021-09-30
Completion
2023-12-01
First posted
2018-12-19
Last updated
2023-09-22

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03781440. Inclusion in this directory is not an endorsement.