Viewing Study NCT04170660


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Ignite Modification Date: 2026-01-03 @ 8:21 PM
Study NCT ID: NCT04170660
Status: UNKNOWN
Last Update Posted: 2023-06-07
First Post: 2019-11-15
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Interest of sFlt1/PlGF Ratio at Obstetric Emergencies
Sponsor: Centre Hospitalier Intercommunal Creteil
Organization:

Study Overview

Official Title: AngioCHIC : Interest of sFlt1/PlGF Ratio at Obstetric Emergencies
Status: UNKNOWN
Status Verified Date: 2023-06
Last Known Status: ACTIVE_NOT_RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: AngioCHIC
Brief Summary: In patients with suspected placental vascular disease who do not require hospitalization, the use of the sFlt-1 (Soluble FMS like tyrosin-kinase-1)/PlGF (Placental Growth Factor)/ assay can most likely help teams to define the best possible management.
Detailed Description: Preeclampsia is a serious obstetric condition, affecting 2 to 5% of pregnancies and associated with maternal hypertension and renal dysfunction. It is a constant concern of obstetrical teams in the pre and post partum period. In case of diagnosis in the emergency unit, patients are usually hospitalized. However, in the case of a diagnosis of preeclampsia has been invalidated, but in presence of isolated or frustrated clinical functional signs, in the case of a history of placental vascular pathology, obstetric teams implement surveillance strategies that are binding on the patients.

The sFlt-1/ PlGF assay has a high negative predictive value for the coming week.

The use in clinical practice of these two biomarkers in the indication of negative prediction at one week could help teams in their management but the interest of this use needs to be evaluated.

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: