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Maternal Inflammatory Parameters Within Routine Treatment With Betamethasone

Preterm Birth Clinical Trial

Official title:
Assessment of Maternal Inflammatory Parameters Within Routine Treatment With Betamethasone Under Threat of Preterm Delivery

Clinical Trial Summary

It is the aim of this study to detect the effect of Betamethasone on the maternal inflammatory parameters C-reactive protein (CRP) and leukocytes of a pregnant woman under threat of preterm delivery, for example because of a cervical infection.

Clinical Trial Description

BACKGROUND

Cortisone influences the maternal number of leukocytes and CRP of a pregnant woman. Because of that, it is difficult to know if the medical treatment of an infection was successful and accordingly if the diagnosis was justified.

METHODS

In this study, the blood results of 75 pregnant women under threat of preterm delivery (week of gestation 23+0 to 34+6), treated with Betamethasone will be analysed. 65 pregnant women without complications serve as control group. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02993744
Study type Observational
Source Medical University of Vienna
Contact
Status Completed
Phase N/A
Start date September 2016
Completion date May 2017
View Details
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