Patients Pregnant Women With or Without Primary Antiphospholipid Antibody Syndrome

RecruitingOBSERVATIONAL
Enrollment

60

Participants

Timeline

Start Date

December 6, 2022

Primary Completion Date

December 6, 2025

Study Completion Date

June 6, 2026

Conditions
PreeclampsiaImmunologic DiseaseAntiphospholipid Antibody Syndrome PrimaryPregnancy ComplicationsPregnancy, High RiskRheumatic Diseases
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.

Trial Locations (1)

Unknown

RECRUITING

San Raffaele Hospital, Milan

All Listed Sponsors
lead

IRCCS San Raffaele

OTHER