Evaluation of Cardiovascular Risk After Preeclampsia in General Practitioners and Patients

NCT ID: NCT06059937

Last Updated: 2025-05-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

155 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-02-26

Study Completion Date

2025-02-11

Brief Summary

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Pre-eclampsia is a disease characterized by placental damage leading to a cascade of complications during pregnancy. It is initially manifested by high blood pressure and the presence of albumin in the urine. It can lead to emergency hospitalization in severe cases and cause major complications or even death in the mother and the fetus.

Several studies observing the outcome of patients with pre-eclampsia have shown an increased long-term cardiovascular risk in these patients, justifying regular medical follow-up with the treating physician and specialists, mainly cardiologists.

The main objective of this research is to describe the cardiovascular risk assessment actions implemented by the treating general practitioner in the year following pre-eclampsia (blood pressure measurement in the office, self-measurement of blood pressure, ABPM, cardiological consultation, biological monitoring of blood (creatininemia, LDL, fasting glycemia) or urine (albuminurie/creatininurie ratio), and screening and management of possible smoking).

Detailed Description

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Conditions

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Patients Hospitalized for Pre-eclampsia

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Interventions

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Patient with pre-eclampsia

Cardiovascular risk assessment by the general practitioner in the year following pre-eclampsia

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients ≥ 18 years hospitalized for preeclampsia at the Nancy regional maternity hospital

Exclusion Criteria

* Fetal death in utero;
* Adult Person subject to a legal protection measure (guardianship, curatorship, safeguard of justice);
* Person deprived of liberty by a judicial or administrative decision;
* Person subject to psychiatric care under constraint by virtue of articles L. 3212-1 and L. 3213-1 of the Public Health Code.
Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

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Central Hospital, Nancy, France

OTHER

Sponsor Role lead

Responsible Party

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Jean-Marc BOIVIN

Principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Nicolas GIRERD, MD-PhD

Role: STUDY_CHAIR

CHRU de NANCY

Locations

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CHRU de NANCY

Vandœuvre-lès-Nancy, , France

Site Status

Countries

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France

Other Identifiers

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2023-A00933-42

Identifier Type: -

Identifier Source: org_study_id

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