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Pharmacokinetic Profile of Aspirin in the Maternal-Fetal Unit and Its Correlation with Pregnancy Outcomes

Pharmacokinetic Profile of Aspirin in the Maternal-Fetal Unit and Its Correlation with Pregnancy Outcomes

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600121013
Enrollment
Unknown
Registered
2026-03-24
Start date
2026-03-30
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

preeclampsia

Interventions

Oral low-dose aspirin group in high-risk population of preeclampsia:NA

Sponsors

Chengdu Third People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. >= 18 years old; 2. Single pregnant women with a high risk group preventive use of aspirin to prevent preeclampsia (high risk factor 3 points/item, medium risk 2 points/item, low risk 1 point/item, total score >= 3 points) are high-risk groups. Risk factor classification: high risk factors: history of preeclampsia, chronic high blood pressure, pregnancy with medical diseases (such as systemic lupus erythematosus, antiphospholipid syndrome, kidney disease, diabetes, etc.), obesity (BMI >= 28.0kg/m ²), pregnant women age >= 40 years old. Medium risk factors: overweight (BMI 24.0~27.9kg/m ²), multiple pregnancies, maternal age 35~10 years, assisted reproductive technology pregnancy, history of gestational hypertension, etc; 3. Can take low-dose aspirin (100 mg/day) orally according to the doctor's advice, and is expected to continue taking the medication until 36 weeks of pregnancy or delivery as directed by the doctor

Exclusion criteria

Exclusion criteria: 1. Contraindications for aspirin: Known allergies to aspirin or other nonsteroidal anti-inflammatory drugs. History of active gastrointestinal ulcers or bleeding. Suffering from asthma, hemophilia, or other hemorrhagic diseases. 2. Combined severe diseases: Combined severe liver and kidney dysfunction (defined as baseline indicators exceeding 1.5 times the upper limit of normal values). Merge uncontrolled hyperthyroidism or hypothyroidism. Combining malignant tumors, severe cardiovascular diseases, neurological disorders, or mental illnesses, unable to cooperate with research. 3. Pregnancy related situation: This pregnancy is a multiple pregnancy conceived through assisted reproductive technology (due to its more complex pharmacokinetics, it can be studied independently). Discovery of significant structural abnormalities or chromosomal abnormalities in the fetus. 4. Combination therapy interference: Long term use of drugs that may interfere with the pharmacokinetics or efficacy of aspirin is required during the study period, such as other anticoagulant/antiplatelet drugs such as low molecular weight heparin, clopidogrel, etc. High dose glucocorticoids. Other nonsteroidal anti-inflammatory drugs (such as ibuprofen, naproxen). 5. Other factors: Researchers determine the presence of any other factors that may interfere with the evaluation of research results or place pregnant women in high-risk situations.

Design outcomes

Primary

MeasureTime frame
Aspirin concentrations;

Secondary

MeasureTime frame
sFlt-1;

Countries

China

Contacts

Public ContactYang Ou

Chengdu Third People's Hospital

1018132349@qq.com+86 182 1552 5083

Outcome results

None listed

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