Fact CheckerSign in

NCT05786235Recruiting

Patients Pregnant Women With or Without Primary Antiphospholipid Antibody Syndrome

Source: ClinicalTrials.gov · Last updated 18 Jun 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Observational
Enrollment
60 (estimated)
First submitted
15 Mar 2023
Start date
6 Dec 2022
Primary completion date
6 Dec 2025
Lead sponsor
IRCCS San Raffaele
NCT number
NCT05786235

What you commit to

  • Study type: Observational
  • Planned participants: 60
  • From 6 Dec 2022 to the primary completion date, 6 Dec 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Group 1
    • PMA pregnancies.
    • Known chronic pathology in gestational period such as chronic essential hypertension, neurological pathology
    • Previous thrombotic event
    • Chronic renal failure not related to AD
    • Previous history of oncology
  • Group 2
    • Pregnancy by PMA.
    • Previous history of polyabortion and/or late pregnancy complications.
    • Known chronic pathology in gestational period such as chronic essential hypertension, neurological pathology
    • Previous thrombotic event
    • Previous history of oncology

Who the study is looking for

  • Group 1
    • Pregnant patients between the ages of 18 and 45 years.
    • Diagnosis of primary APS, according to international classification criteria.
  • Group 2
    • Pregnant patients between the ages of 18 and 45 years.
    • Patients with at least one previous full-term pregnancy.
    • No diagnosis of APS, according to international classification criteria.

Age in the registry: 18 years to 45 years · Sex: Female · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
San Raffaele Hospital
Coordinator of this site? Confirm its status
MilanItalyRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.