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NCT03611374

Regional Anesthesia for Cardiothoracic Enhanced Recovery (RACER) Study

Completed NA Last updated 28 September 2023
What this trial tests

NA trial testing Bilateral Erector Spinae Plane Block (ESPB) in Congenital Heart Defect in 38 participants. Completed in 6 April 2023.

Timeline
7 June 2019
Primary endpoint
6 April 2023
6 April 2023

Quick facts

Lead sponsorStanford University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment38
Start date7 June 2019
Primary completion6 April 2023
Estimated completion6 April 2023
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Stanford University

Who can join

Adults 0 to 99, any sex, with Congenital Heart Defect or Congenital Heart Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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).

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Congenital Heart Defect

Currently open trials in the same condition.

Other Stanford University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03611374.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing