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Evaluation of Cardiovascular Risk After Preeclampsia in General Practitioners and Patients (PreCarVasc)

C

Central Hospital, Nancy, France

Status

Completed

Conditions

Patients Hospitalized for Pre-eclampsia

Treatments

Other: Patient with pre-eclampsia

Study type

Observational

Funder types

Other

Identifiers

NCT06059937
2023-A00933-42

Details and patient eligibility

About

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).

Enrollment

155 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

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.

Trial contacts and locations

1

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Central trial contact

Jean Marc Boivin, MD-PhD; Georges Weryha, MD-PhD

Data sourced from clinicaltrials.gov

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