Overview

Continuous Erector Spinae Block Versus Continuous Paravertebral Block

Status:
Recruiting
Trial end date:
2022-07-01
Target enrollment:
0
Participant gender:
All
Summary
Overall Aim: To evaluate the efficacy of continuous erector spinae block (ESB) versus continuous paravertebral block (PVB) for postoperative analgesia in children and adolescents undergoing surgical procedures via unilateral thoracotomy. Hypothesis: The investigators hypothesize that ESP block efficacy is not inferior to that of PVB with respect to pain control and consumed opiate equivalents at 24 hours postoperatively.
Phase:
Phase 3
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Boston Children's Hospital
Boston Children’s Hospital
Treatments:
Ropivacaine
Criteria
Inclusion Criteria:

- ASA I - III status, undergoing unilateral thoracotomy for either esophageal atresia
related intrathoracic procedures or other non-cardiac general surgical intrathoracic
procedures.

Exclusion Criteria:

- Patients undergoing procedures including pleurodesis, pleural stripping, and
decortication or other procedures with widely distributed pleural disruption.

- Patients with severe neurodevelopmental delays.

- Patients with previous chronic pain syndromes.

- Patients with a history of opioid treatment at any point in the 2 months prior to
surgery.

- Lack of parental consent and/or child assent.