Status:
TERMINATED
Continuous Erector Spinae Block Versus Continuous Paravertebral Block
Lead Sponsor:
Boston Children's Hospital
Conditions:
Pain, Postoperative
Eligibility:
All Genders
6-6 years
Phase:
PHASE3
Brief 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 p...
Detailed Description
Regional anesthesia-and pediatric regional anesthesia in particular-is a rapidly evolving subfield of anesthesia practice driven with considerable urgency by the growing recognition that even appropri...
Eligibility Criteria
Inclusion
- ASA I - III status, undergoing unilateral thoracotomy for either esophageal atresia related intrathoracic procedures or other non-cardiac general surgical intrathoracic procedures.
Exclusion
- 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.
Key Trial Info
Start Date :
April 16 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
February 1 2025
Estimated Enrollment :
100 Patients enrolled
Trial Details
Trial ID
NCT03768440
Start Date
April 16 2019
End Date
February 1 2025
Last Update
February 17 2025
Active Locations (1)
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1
Boston Children"S Hospital
Boston, Massachusetts, United States, 02118