Ireland
--:--IST
Latest
Clinical Trials in France / NCT05056701
Recruiting Not applicable

Prediction of Chronic Kidney Disease Following Pre-eclampsia: Diagnosis and Early Care

NCT05056701 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2022-05-30
Last updated
2024-09-04

Condition(s) studied

Preeclampsia

Investigational drug(s) / intervention(s)

annual follow-up during 10 years

annual follow-up during 10 years: an annual follow-up is carried out systematically for a total of 10 years in order to detect the subsequent occurrence of CKD

Study summary

Pre-eclampsia (PE) is a pregnancy-associated syndrome of variable severity, classically defined by the combination of hypertension and proteinuria in a previously non-hypertensive or proteinuric patient. These symptoms normally resolve within 2-3 months after delivery regardless of the severity of the pre-eclampsia.

Regardless of its definition, preeclampsia is associated with an increased risk of obstetric events and, for the mother, an increased risk of developing chronic kidney disease (CKD), hypertension, diabetes and cardiovascular disease in the broad sense.

The relationship between preeclampsia and Chronic Kidney Disease is, however, complex and not fully understood.

Investigator proposes an interventional study to identify the diagnosis of Chronic Kidney Disease in patients who have developed an episode of Preeclampsia.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Meeting the preeclampsia criteria or one of its complications (eclampsia, HELLP syndrome) according to the ISSHP 2018 definitions within the last 5 years * Having signed the informed consent * Person affiliated to social security Exclusion Criteria: * Patient with mental disability or language barrier preventing understanding of the study or consent * Person deprived of liberty by judicial or administrative decision * Person under forced psychiatric care * Person subject to a legal protection measure

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Chu Angers Angers France Not Yet Recruiting
Centre Hospitalier Du Mans Le Mans France Recruiting

More Centre Hospitalier le Mans trials in France

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05056701 on ClinicalTrials.gov ↗ ← All trials in France