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Bilateral Continuous Erector Spinae Blocks for Post-Sternotomy Pain Management

NCT04567407 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 45

Last updated 2023-10-17

Study results available
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Summary

To evaluate the efficacy of bilateral continuous erector spinae blocks (BESB) for postoperative analgesia in children and adolescents undergoing cardiac surgical procedures via sternotomy in the Early Recovery After Surgery (ERAS) program in a single arm, open label, interventional study.

Conditions

  • Postoperative Pain

Interventions

DRUG

Bilateral erector spinae blocks using ropivacaine

Bilateral chest wall nerve blocks using ropivacaine.

Sponsors & Collaborators

Principal Investigators

  • ROLAND BRUSSEAU, MD · Boston Children's Hospital

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
2 Years
Max Age
17 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-09-22
Primary Completion
2022-01-22
Completion
2022-01-22
FDA Drug
Yes

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04567407 on ClinicalTrials.gov