tility of noninvasive regional saturation monitoring using with INVOS500 to predict prognosis in pediatric patients with congenital heart disease
Not Applicable
Recruiting
- Conditions
- congenital heart disease
- Registration Number
- JPRN-UMIN000031183
- Lead Sponsor
- Department of Anesthesiology, Hirosaki University Graduate School of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
Not provided
Exclusion Criteria
body weight over 10 kg
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Poor outcomes including 30-day mortality, duration of ICU stay, duration of respiratory ventilation, administration of renal replacement therapy and ECMO
- Secondary Outcome Measures
Name Time Method