preeclampsia
Conditions
Interventions
Case series:none
control group:none
Sponsors
Beijing Obstetrics and Gynecology Hospital, Capital Medical University
Eligibility
Sex/Gender
Female
Age
18 Years to 45 Years
Inclusion criteria
Inclusion criteria: 1.Age 18-45 years; 2.Single pregnant women; 3.Clinically assessed to be at high risk of preeclampsia and requiring low-dose aspirin prophylaxis; 4.Women who have registered with our hospital, undergone regular prenatal check-ups, and plan to give birth at our hospital; 5.Pregnant women who voluntarily participate in this study and sign the informed consent form;
Exclusion criteria
Exclusion criteria: 1.Gestational age exceeding 16 weeks at enrollment; 2.Allergy or contraindication to aspirin or other non-steroidal anti-inflammatory drugs (such as active bleeding, severe peptic ulcer); 3.Individuals with clear anticoagulant indications requiring anticoagulant therapy; 4.Individuals with comorbidities affecting platelet function, such as cardiovascular disease and autoimmune disease; 5.Unable to provide complete prenatal care records; 6.Significant fetal structural abnormalities or fetal malformations;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| preeclampsia;predictive performance; | — |
Secondary
| Measure | Time frame |
|---|---|
| model extrapolation; | — |
Countries
China
Contacts
Public ContactChen Yi
Beijing Obstetrics and Gynecology Hospital, Capital Medical University
Outcome results
None listed