Registry for kidney health during pregnancy

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to collect data on women with kidney diseases and their experiences during pregnancy. It focuses on understanding how pre-existing kidney conditions affect pregnancy outcomes and maternal health. The study will extract data from medical files of women at different stages: pre-conception, during pregnancy, and postpartum. By analyzing this data, researchers hope to identify complications and improve care for pregnant women with kidney issues.

Why it matters

Who can join: the full rules

Inclusion Criteria:

1. Pre-conception consultations

   Woman of childbearing age with:
   * Renal damage (glomerular, tubular disease, renal lithiasis, systemic disease, metabolic diseases, congenital diseases, etc.)
   * Hematological disorders (sickle cell disease)
   * Kidney transplantation
   * High blood pressure (hypertension)
   * Pre-kidney transplant assessment in progress for discussion of contraception and pregnancy after kidney transplantation
   * Preeclampsia
   * Multiple miscarriages
   * IUGR and low birth weight in the fetus
   * Family history of kidney disease
2. Peri-gravid consultations

   Pregnant women with
   * Pre-existing kidney damage
   * De novo renal failure (IR)
   * Proteinuria
   * Hematuria
   * Chronic hypertension
   * Pregnancy hypertension
   * Renal lithiasis
3. Postpartum consultations

Postpartum women with

* Early/late pre-eclampsia
* Eclampsia / Hemolysis Elevated Liver enzymes Low Platelet (HELLP) syndrome
* Pregnancy hypertension
* Postpartum hemorrhage
* De novo renal failure postpartum

Exclusion Criteria:

Male patients Menopausal patients

Where it's running

• CHU Brugmann
  Brussels, Belgium Recruiting

Study contacts

• Principal investigator: Christelle Fosso — CHU Brugmann
• Study coordinator: Christelle Fosso
• Email: Christelle.FOSSO@chu-brugmann.be
• Phone: 3224772016

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.