controlled study between erector spinea plane block versus paravertebral nerve block in neonates undergoing tracheo-esophageal fistula repair
Phase 4
Recruiting
- Conditions
- Neonatal DiseasesAnaesthesia
- Registration Number
- PACTR201908568919626
- Lead Sponsor
- Faculty of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
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.