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Amniotic Fluid Optical Density Determination as a Test for Assessment of Fetal Lung Maturity.

Respiratory Distress Syndrome, Newborn Clinical Trial

Official title:
Amniotic Fluid Optical Density Determination Between 28 and 36 6/7 Weeks of Pregnancy and Its Relationship With the Diagnosis of Neonatal Respiratory Distress Syndrome.

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

Clinical Trial Details
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
View Details
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