Patent ductus arteriosus and Left Atrial Size Evaluation study in preterm infants (multicenter prospective observational cohort study without interventions)
- Conditions
- preterm infants
- Registration Number
- JPRN-UMIN000016280
- Lead Sponsor
- Patent ductus arteriosus and Left Atrial Size Evaluation study in preterm infants (PLASE) Study Group
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 710
Not provided
Chromosomal abnormality:(13, 18, 21 trisomy, del 22q11.2, Noonan syndrome, etc). Multiple anomalies, apparent clinical syndrome, congenital anomalies which needs operation during infancy. Congenital heart disease other than PDA/PFO/PLSVC. Congenital metabolic disease, endocrinologic disease, neuromuscular disease, systemic bone disease. Family history of severe heredity disease such as neuromuscular disease or cardiomyopathy. Neonates whose parents do not agree to provide the patients' data to the study. Critical condition ineligible for this study, which was judged by attending physician.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method