controlled study between erector spinea plane block versus paravertebral nerve block in neonates undergoing tracheo-esophageal fistula repair

Phase 4

Recruiting

• Conditions: Neonatal Diseases; Anaesthesia

• Registration Number: PACTR201908568919626
• Lead Sponsor: Faculty of Medicine

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2019-06-19
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

Patients selected will be of both sexes aged 1 to 30 days
scheduled for tracheo-esophageal fistula repair surgery.

Exclusion Criteria

Patients known to be allergic to any of the study drugs,
known or suspected coagulopathy or recent use of anticoagulant/antiplatelet drugs,
any signs of infection, congenital abnormalities of spine and meninges, empyema.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The primary aim is to compare ultrasound guided erector spinae plane block vs paravertebral nerve block for narcotic and anesthetic consumption in neonates undergoing tracheo-esophageal fistula repair.

Secondary Outcome Measures

Name	Time	Method
The secondary aim is to measure hemodynamic changes, postoperative analgesic consumption, and incidence of complications.