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Clinical Trial Summary

To determine the relationship between the result of amniotic fluid optical density between 26 and 36 6/7 weeks of pregnancy and the risk of developing neonatal respiratory distress syndrome.


Clinical Trial Description

n/a


Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


NCT number NCT02332304
Study type Interventional
Source Saint Thomas Hospital, Panama
Contact
Status Completed
Phase Phase 3
Start date May 2014
Completion date December 2014

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