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NCT05151289: ANGIOPAG

Diagnostic Value of sFlt-1/PlGF Ratio for the Etiology of Intra Uterine Growth Restriction - ANGIOPAG

Status unknown NA Last updated 9 December 2021
What this trial tests

NA trial testing Blood test at time of inclusion for sFlt-1/PlGF ratio in Intrauterine Growth Restriction in 152 participants. Status unknown.

Timeline
8 January 2020
Primary endpoint
29 January 2022
29 January 2022

Quick facts

Lead sponsorAssistance Publique - Hôpitaux de Paris
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposediagnostic
Enrollment152
Start date8 January 2020
Primary completion29 January 2022
Estimated completion29 January 2022
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

Assistance Publique - Hôpitaux de Paris — full company profile →

Who can join

18 and older, female only, with Intrauterine Growth Restriction or Fetal Growth Restriction (FGR). Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The main aim of this project is to determine the Placental Growth Factor and Vascular Endothelial Growth Factor ratio's performance (sFlt-1/PlGF) for the etiological diagnosis of vascular Intrauterine growth restriction (IUGR) compared to a non-vascular IUGR.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Intrauterine Growth Restriction

Currently open trials in the same condition.

Other Assistance Publique - Hôpitaux de Paris trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05151289.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing