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RECRUITING
NCT05786235

Patients Pregnant Women With or Without Primary Antiphospholipid Antibody Syndrome

Sponsor: IRCCS San Raffaele

View on ClinicalTrials.gov

Summary

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.

Key Details

Gender

FEMALE

Age Range

18 Years - 45 Years

Study Type

OBSERVATIONAL

Enrollment

60

Start Date

2022-12-06

Completion Date

2026-06-06

Last Updated

2025-06-18

Healthy Volunteers

Yes

Interventions

OTHER

Collection of epidemiological and anamnestic data and collection of biological material (peripheral blood)

Patients will be enrolled in the study during the first trimester of gestation or later, if the diagnosis of APS is made during pregnancy followed by clinical practice. During the quarterly visits scheduled by clinical practice, the following will be collected relevant clinical information and the additional biological samples for analysis of serum levels of sFlt-1 and PlGF. A follow-up postpartum visit is scheduled by clinical practice at 6 weeks after completion of delivery.

OTHER

Collection of epidemiological and anamnestic data and collection of biological material (peripheral blood)

Patients will be enrolled during the performance of prenatal diagnosis, routinely chosen by the patient, at which the relevant clinical information and the additional biological sample . Collection of biological material in the 2nd and 3rd TM of gestation will take place at occasion of the routinely scheduled ultrasound scans . A postpartum follow-up visit is scheduled by clinical practice at 6 weeks after the completion of delivery.

Locations (1)

San Raffaele Hospital

Milan, Italy