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Study identifier: NCT05786235 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Patients Pregnant Women With or Without Primary Antiphospholipid Antibody Syndrome

Condition: Preeclampsia · Immunologic Disease · Antiphospholipid Antibody Syndrome Primary  ·  Sponsor: IRCCS San Raffaele

PhaseN/A
Planned participants60
Who can joinFemale, 18 Years to 45 Years
Healthy volunteersYes

About this study

The purpose of the study is to evaluate the ability of placental angiogenesis markers to predict the risk of PE in pregnancy in women with primary APS. To construct reference intervals of placental angiogenesis markers specific to women affected by primary APS in pregnancy by measuring the levels of sFlt-1and PlGF in serum maternal serum and their sFlt-1/PlGF ratio during the trimesters of gestation (I TM, II TM and III TM). For this aim the study will involve recruiting two groups of subjects, one will be cases and one will be controls.

This description comes directly from the study's public registry record.

Talk to the study team

Patrizia Rovere Querini  ·  +390226436095  ·  rovere.patrizia@hsr.it

Valentina Canti  ·  +390226436095  ·  canti.valentina@hsr.it

Always discuss trial participation with your own doctor first.

Locations (1)

San Raffaele HospitalMilan, ItalyRecruiting

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Source record: clinicaltrials.gov/study/NCT05786235