Actively Recruiting
Prediction of Chronic Kidney Disease Following Pre-eclampsia: Diagnosis and Early Care
Led by Centre Hospitalier le Mans · Updated on 2024-09-04
400
Participants Needed
2
Research Sites
782 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Prediction of Chronic Kidney Disease Following Pre-eclampsia: Diagnosis and Early Care
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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
You will not qualify if you...
- 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
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 2 locations
1
Chu Angers
Angers, France, 49000
Not Yet Recruiting
2
Centre Hospitalier Du Mans
Le Mans, France, 72000
Actively Recruiting
Research Team
C
Christelle JADEAU
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
PREVENTION
Number of Arms
1
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