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A Study on the Diagnostic Value of Multimodal Ultrasound Combined with Metabolomics in Thrombophilia-Related Placental Pathological Pregnancies

A Study on the Diagnostic Value of Multimodal Ultrasound Combined with Metabolomics in Thrombophilia-Related Placental Pathological Pregnancies

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600117058
Enrollment
Unknown
Registered
2026-01-19
Start date
2026-01-20
Completion date
Unknown
Last updated
2026-01-27

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

Conditions

thrombophilia

Interventions

Thrombophilia Pregnant Women Group:None

Sponsors

The Second Affiliated Hospital of Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria for the Thrombophilia Group: 1. Pregnant women aged 18–45 years; 2. Meeting diagnostic criteria for hereditary or acquired thrombophilia as outlined in the Chinese Guidelines for Diagnosis and Prevention of Thrombophilia (2021 Edition) (e.g., persistent positive antiphospholipid antibodies, protein C/S deficiency, antithrombin deficiency, specific gene mutations, etc.); 3. Single gestation; 4. Informed consent provided and willingness to complete all examinations and follow-up procedures required for this study. Healthy Pregnant Women Group Inclusion Criteria: 1. Healthy pregnant women with gestational age matching that of the case group; 2. No known history of thrombophilia or laboratory evidence thereof; 3. Absence of comorbidities potentially affecting cardiovascular function, such as autoimmune diseases, chronic hypertension, diabetes mellitus, or renal disease; 4. No long-term medication use that may impact coagulation or cardiovascular function (e.g., corticosteroids, immunosuppressants).

Exclusion criteria

Exclusion criteria: 1. Severe concomitant non-cardiovascular conditions (such as active infections, malignant tumours, or severe hepatic or renal insufficiency); 2. History of smoking, alcohol consumption, or use of medications significantly impacting pregnancy outcomes; 3. Incomplete clinical data, suboptimal ultrasound image quality, or other factors precluding effective analysis.

Design outcomes

Primary

MeasureTime frame
Diagnostic criteria for thrombophilia (antiphospholipid antibodies, protein C, protein S, homocysteine, etc.);Blood biomarkers (blood glucose, blood lipids, placental growth factor (PlGF), folic acid, vitamin D, hCG, etc.);Metabolomics (serum, urine, and placental tissue);Multimodal ultrasound imaging (placental perfusion assessment, maternal cardiac and carotid ultrasound examinations, foetal cardiac ultrasound examinations, foetal organ perfusion assessments, uterine artery studies, routine antenatal ultrasound measurements, etc.);General Clinical Data (Blood Pressure, BMI, etc.);

Countries

China

Contacts

Public ContactHongxia Yu

The Second Affiliated Hospital of Zhengzhou University

xiaochb@163.com+86 156 3887 2360

Outcome results

None listed

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