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Patent ductus arteriosus and Left Atrial Size Evaluation study in preterm infants (multicenter prospective observational cohort study without interventions)

Not Applicable
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
Inclusion Criteria

Not provided

Exclusion Criteria

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
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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