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Molecular Study of the Maternal-fetal Interface in Preeclampsia.
Sponsor: Carlos Simon Foundation
Summary
Preeclampsia (PE) is a major obstetric complication with short- and long-term consequences for the mother and the fetus. Early screening tools to reduce its mortality and morbidity, as well as to prevent the life-threatening consequences are needed. Thus, the detection of women at risk of suffering PE is key to apply preventive and treatment strategies. Recently, the maternal contribution to PE based on defective decidualization that prevents the establishment of a functional maternal-fetal interface has been evidenced. The main objective of this study is to identify molecular markers or aberrant maternal-fetal cell types that can be detected early in the development of the disease in maternal-fetal interface tissue (chorionic villi + decidua) collected during gestational weeks 9 to 15. Maternal-fetal interface biopsy will be collected from women who have a recommendation for aneuploidy testing. The remaining fragment will be used for this study.
Official title: Molecular Study of the Maternal-fetal Interface Prospectively to the Onset of Preeclampsia Using Single Cell Technology.
Key Details
Gender
FEMALE
Age Range
18 Years - Any
Study Type
OBSERVATIONAL
Enrollment
2084
Start Date
2023-11-20
Completion Date
2027-12
Last Updated
2025-12-23
Healthy Volunteers
Not specified
Conditions
Interventions
Maternal-fetal interface biopsy and peripheral blood collection in cases group
Maternal-fetal interface tissue (chorionic villi and decidua) will be collected from women who have a recommendation for aneuploidy testing, and the remaining fragment will be used for this study and peripheral blood collection in cases group. Clinical data will be compiled.
Maternal-fetal interface biopsy and peripheral blood collection in control group
Maternal-fetal interface tissue (chorionic villi and decidua) will be collected from women who have a recommendation for aneuploidy testing, and the remaining fragment will be used for this study and peripheral blood collection in control group. Clinical data will be compiled.
Locations (5)
Hospital General Universitario Dr. Balmis
Alicante, Alicante, Spain
Hospital Universitario de Torrejón
Madrid, Madrid, Spain
Hospital Clinico Universitario Virgen de la Arrixaca
Murcia, Murcia, Spain
Hospital Universitario de Canarias
Santa Cruz de Tenerife, Santa Cruz de Tenerife, Spain
Hospital Universitario y Politécnico La Fe
Valencia, Valencia, Spain