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Evaluation of the Safety and Performance of Centaflow

Fetal Growth Restriction Clinical Trial

Official title:
Evaluation of the Safety and Performance of Centaflow as a Routine Assessment of Placental Vascular Function and Foetal Cardiovascular Health

Clinical Trial Summary

The aim of this study is to evaluate the safety and performance of an acoustic approach based on skin-contact microphones as a routine assessment of placental vascular function as predictor of fetal growth restriction.

Clinical Trial Description

Evaluation of the safety and performance of Centaflow as routine antenatal assessment of placental vascular function as predictor of fetal growth restriction is performed by randomizing singleton pregnant women with ultrasound-based gestations for either standard care (SC) or SC and Centaflow (CF). The subjects will be randomized in ratio 1:1 in both groups and examined in pregnancy weeks 27-29, 34-36 and 37-39. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04438668
Study type Interventional
Source Centaflow
Contact Richard Farlie, MD, MI, MHM
Phone +45 78 44 58 63
Email richard.farlie@midt.rm.dk
Status Recruiting
Phase N/A
Start date June 3, 2020
Completion date June 30, 2022
View Details
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