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Clinical characteristics and risk factors of non-criteria obstetric antiphospholipid syndrome with preeclampsia analysis

Clinical characteristics and risk factors of non-criteria obstetric antiphospholipid syndrome with preeclampsia analysis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500095848
Enrollment
Unknown
Registered
2025-01-14
Start date
2025-01-20
Completion date
Unknown
Last updated
2025-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

non-criteria obstetric antiphospholipid syndrome

Interventions

Group of non-standard antiphospholipid syndrome and preeclampsia:None
Control group:None

Sponsors

Shijiazhuang Fourth Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: (1) Pre eclampsia meets the diagnostic criteria of the 9th edition of the Obstetrics and Gynecology textbook, while patients with non-standard obstetric antiphospholipid syndrome meet the definition of NCOAPS in the "Expert Consensus on Diagnosis and Management of Obstetric antiphospholipid Syndrome". They only meet the clinical or laboratory criteria in the APS classification criteria, including: clinical manifestations that meet the APS criteria, atypical laboratory tests (2 aPL positive but with a detection interval of less than 12 weeks), IgG/IgM type anticardiolipid (aCL), and/or he titer of anti - ß 2-GPI antibody is 20-39GPL/MPL or 95-99th percentile); Or laboratory tests meet APS criteria, with atypical clinical manifestations (2 consecutive unexplained abortions; or 3 or more non consecutive unexplained abortions; or late-onset preeclampsia; or placental hematoma, placental abruption, late preterm birth). (2) Complete clinical data. (3) Anticardiolipin antibodies (ACA), lupus anticoagulant, anti - ß 2 glycoprotein I antibodies, and D2 oligomers were detected between 12-16 weeks of pregnancy and before delivery.

Exclusion criteria

Exclusion criteria: (1) Multiple pregnancies; (2) Fetal chromosomal abnormalities and structural abnormalities; (3) Pregnancy loss caused by infection, metabolic factors, endocrine factors, chromosomal abnormalities, anatomical abnormalities, and other reasons; (4) Merge other systemic autoimmune diseases; (5) Combining hereditary thrombophilia or nephrotic syndrome, malignant tumors, and other acquired thrombophilia; (6) Merge hepatitis B virus, hepatitis C virus, and human immunodeficiency virus infections.

Design outcomes

Primary

MeasureTime frame
Anticardiolipin antibody;Anti - ß 2 glycoprotein 1 antibody;lupus anticoagulant;blood pressure;

Secondary

MeasureTime frame
platelet;family history;History of hypertension in the past;body mass index;age;Maternity history;urinary protein;D-Dimer;

Countries

China

Contacts

Public ContactMeng Yancen

Shijiazhuang Fourth Hospital

251055159@qq.com+86 150 3216 1008

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026