Actively Recruiting

Age: 18Years - 45Years
FEMALE
Healthy Volunteers
ID03313024

Characterization of Immune Cell and Placental Cell Interaction in Pregnancy Disorders

Led by Charite University, Berlin, Germany · Updated on 2018-08-14

1580

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying how different immune cells interact with placental cells and how this interaction may lead to pregnancy complications, especially focusing on preeclampsia. The study aims to understand how uteroplacental syndrome develops into maternal symptoms in preeclampsia by examining immune cell subtypes that cause endothelial dysfunction and cardiovascular damage during pregnancy. This observational study includes healthy pregnant women as well as those diagnosed with preeclampsia, gestational hypertension, or gestational diabetes. Participants will be observed without receiving experimental treatments. The study focuses on comparing immune cell populations, particularly T cells, at the time of preeclampsia diagnosis to those in control pregnancies. Participants will undergo evaluations including flow cytometry to measure T cell populations during pregnancy. Researchers will collect data at the time of preeclampsia diagnosis and compare it with controls at the same gestational stage. The study is sponsored by Charite University in Berlin and includes women aged 18 to 45 years. The total participation duration varies by the timing of diagnosis and pregnancy progress.

CONDITIONS

Brief Title

Berlin-Brandenburg Pregnancy Cohort

Who Can Participate

Age: 18Years - 45Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Healthy pregnant women who have given informed consent
  • Pregnant women diagnosed with preeclampsia, gestational hypertension, or gestational diabetes
Not Eligible

You will not qualify if you...

  • Presence of infections
  • Alcohol or drug abuse
  • Manifest or chronic diseases

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

Duration - Throughout pregnancy until diagnosis or delivery

Participants undergo assessments to characterize immune and placental cell interactions during pregnancy disorders.

Multiple visits during pregnancy depending on condition

Long-term Monitoring

Duration - Up to delivery and postpartum period

Participants are observed over time to monitor immune cell populations and pregnancy outcomes.

Periodic visits during and after pregnancy

Trial Site Locations

Total: 1 location

1

Experimental and Clinical Research Center (ECRC)

Berlin, Germany, 13125

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Research Team

F

Florian Herse, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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