Skip to content

Regional Anesthesia for Cardiothoracic Enhanced Recovery (RACER) Study

Regional Anesthesia for Cardiothoracic Enhanced Recovery (RACER) for Patients Undergoing Sternotomy for Congenital Heart Repair

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03611374
Enrollment
38
Registered
2018-08-02
Start date
2019-06-07
Completion date
2023-04-06
Last updated
2023-09-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anesthesia, Local, Congenital Heart Defect, Congenital Heart Disease, Opioid Use

Brief summary

The erector spinae plane block is a novel regional anesthetic technique that allows for analgesia of the thorax and abdomen with a peripheral nerve block. The goals of this study are to determine if bilateral erector spinae plane blocks (ESPB) after sternotomy for congenital heart repair in high risk children and adults can decrease outcomes such as duration of postoperative mechanical ventilation (MV), perioperative opioid consumption, days in the intensive care unit (ICU) and length of stay (LOS).

Interventions

PROCEDUREBilateral Erector Spinae Plane Block (ESPB)

Bilateral ESPBs will be placed after anesthesia induction in eligible and consented patients who are undergoing a sternotomy for congenital heart repair. Patients will receive a local anesthetic agent through each catheter prior to surgery start. If possible, levels of the local anesthetic will be measured during the case. After surgery, patients will be admitted to the CVICU and extubation will be managed by the CVICU team. The ESPB group will have an automatic, alternating side boluses of the local anesthetic started through their nerve block catheters. Levels of the local anesthetic will be measured at intervals.

Sponsors

Stanford University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
0 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

i) Ages 0-99 ii) Give consent/parental consent to participate in study iii) Patients undergoing sternotomy for congenital heart repair surgeries

Exclusion criteria

i) Participants who do not consent or have parental consent ii) Patients who are clinically unstable or require urgent/emergent intervention iii) Patients under 5kg

Design outcomes

Primary

MeasureTime frame
Median time to extubation in patients with ESPBDuration of postoperative recovery (typically 1-2 weeks)
Median Cardiovascular Intensive Care Unit (CVICU) LOS in patients with ESPBDuration of postoperative recovery (typically 1-2 weeks)
Determine average post-operative pain scores in patients with ESPBDuration of postoperative recovery (typically 1-2 weeks)
Determine opioid consumptionDuration of postoperative recovery (typically 1-2 weeks)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026