Predicting effective and safe fluid removal by furosemide bolus administration in critically ill neonates and infants
Not Applicable
- Conditions
- on-cardiac critically ill neonates and infants
- Registration Number
- JPRN-UMIN000041048
- Lead Sponsor
- Saitama Children's Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 23
Inclusion Criteria
Not provided
Exclusion Criteria
Furosemide boluses in patients meeting any of the following criteria were excluded: 1) patients undergoing any type of dialysis; 2) history of any type of congenital heart disease; 3) presence of complications known to affect urinary output, such as diabetes insipidus or severe hyperglycemia; 4) use of other diuretics (including furosemide) within 6 h preceding the index furosemide bolus; or 5) use of any kind of extra-corporeal circulation.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method