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Age: 18Years +
FEMALE
ID06779916

Study on the Balance of Cell Processes in Placental Blood Vessel Complications During Pregnancy

Led by Centre Hospitalier Universitaire de Nīmes · Updated on 2026-05-06

50

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Pregnancy raises the risk of blood clots and complications related to the placenta, which can cause serious health issues for both mother and baby. Researchers are studying the balance between autophagy cell maintenance and apoptosis cell death in the placenta to better understand how these processes may contribute to placental vascular diseases like preeclampsia and intrauterine growth retardation. This study builds on previous research that looked at these cell activities in normal pregnancies. The study involves pregnant women who develop placental vascular complications and are hospitalized at Nimes University Hospital. Blood and urine samples will be collected at the start, then monthly during pregnancy follow-up visits, and again at delivery. These samples will be tested to measure specific proteins related to autophagy and apoptosis, as well as other markers linked to vascular and kidney function. Participants will undergo regular monitoring through blood and urine tests to track changes in cell activity and other biological markers from the start of the study until delivery. Researchers will analyze these samples to understand the cellular mechanisms involved in the placental complications. The study aims to provide new insights that could lead to better screening and prevention strategies for these pregnancy-related vascular problems.

CONDITIONS

Brief Title

Autophagy/Apoptosis Balance in Placental Vascular Pathologies

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Pregnant women developing a placental vascular complication such as preeclampsia and/or intrauterine growth retardation, hospitalized and delivering at Nimes University Hospital
  • Pregnant women who provide free and informed consent
  • Pregnant women affiliated with or benefiting from a health insurance scheme
Not Eligible

You will not qualify if you...

  • Multiple pregnancy
  • Presence of hypertension and/or proteinuria before pregnancy
  • Participation in any interventional drug study
  • Being excluded due to another study's rules
  • Persons under court protection, guardianship, or curatorship
  • Persons unable to give consent
  • Persons for whom it is impossible to provide informed information

Research Team

S

Sylvie BOUVIER, Dr.

A

Anissa MEGZARI

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