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The Prognostic Value of Cervical Elastography for Identifying Patients at Risk for Preterm Delivery — ElastoMAP  

Obstetric Labor, Premature Clinical Trial

Official title:
The Prognostic Value of Cervical Elastography for Identifying Patients at Risk for Preterm Delivery

Clinical Trial Summary

The hypothesis tested is that the physical changes associated with cervical ripening result in a detectable decrease in rigidity. The main objective of this study is therefore to determine whether the measured elastographic rigidity of cervical tissues in addition to cervix size can be used to predict delivery within the next 48 hours (creation of a prognostic score).

Clinical Trial Description

The secondary objectives of this study are:

A-To compare the prognostic qualities of elastography scores and fetal fibronectin measurements for predicting the risk of delivery in the next 48 hours.

B-To evaluate the economic impact of introducing elastographic and fibronectin measures during consultatios for obstetric emergencies from the point of vue of the French social security system and the hospital.

C-To evaluate the prognostic value of elastographic measurements in the subgroup twins.

D-To study elastography variation according to patient outcomes.

E-Evaluate the reproducibility of intra-and inter-rater elastographic measurements. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02021539
Study type Observational
Source Centre Hospitalier Universitaire de Nimes
Contact
Status Terminated
Phase N/A
Start date February 2014
Completion date December 2016
View Details
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