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Clinical Trial Summary

This is a multicentre, open-label, randomized controlled trial. A total of 598 singleton pregnancies with an EFW ≤10th percentile at <32+0 weeks will be recruited and randomly allocated to either the control or the intervention group. In the control group, standard Doppler-based management will be used. In the intervention group, different soluble fms-like tyrosine kinase to placental growth factor ratio (sFlt-1/PlGF) cutoffs will be incorporated to the current protocol to adjust the frequency of ultrasounds and to plan elective delivery.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05284474
Study type Interventional
Source Hospital Universitari Vall d'Hebron Research Institute
Contact Manel Mendoza, MD, PhD
Phone +34934893000
Email mmendoza@vhebron.net
Status Not yet recruiting
Phase N/A
Start date September 1, 2022
Completion date January 30, 2025

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