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Risk prediction and prevention of serious pregnancy complications in pregnant women with hypertensive disorders of pregnancy

Risk prediction and prevention of serious pregnancy complications in pregnant women with hypertensive disorders of pregnancy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100048266
Enrollment
Unknown
Registered
2021-07-05
Start date
2022-01-01
Completion date
Unknown
Last updated
2022-03-14

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

Conditions

Hypertensive disorders of pregnancy

Interventions

case series:None

Sponsors

Women's Hospital, School of Medicine, Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1. Evaluation of the effect of aspirin in preventing preeclampsia and serious pregnancy complications: (1) 11-13+6 gestational weeks; (2) Aged >=18 years; (3) Singleton pregnancy, the fetus survives; (4) Agree to participate and sign the informed consent form. 2. Establishment of a risk prediction model for severe pregnancy complications in hypertensive disorders of pregnancy: (1) 20-36+6 gestational weeks; (2) Diagnosed with >= 1 of the following diseases: gestational hypertension, preeclampsia, pregnancy complicated with chronic hypertension, chronic hypertension with preeclampsia; (3) Aged >18 years; (4) Singleton pregnancy, fetal survival; (5) Agree to participate and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Evaluation of the effect of aspirin in preventing preeclampsia and serious pregnancy complications: (1) Serious fetal malformation/abnormality; (2) Routine use of aspirin before enrollment; (3) Aspirin contraindications such as salicylic acid allergy, peptic ulcer disease, bleeding history, liver cirrhosis, renal failure, platelet count <50x10^9/L, hematocrit <10%, hemophilia, congenital platelets disease, fibrinogen deficiency or deficiency, use of antiplatelet drugs other than aspirin, use of anti-inflammatory drugs, or use of warfarin; (4) Those who have been diagnosed with pregnancy-induced hypertension; (5) Severe mental disorders, unable to express their wishes; (6) There are obvious other abnormal signs, laboratory examinations and other clinical diseases, and according to the judgment of the researcher, they are not suitable to participate in the researcher; (7) According to the investigator's judgment, it is impossible to observe and follow-up to obtain delivery information. 2. Establishment of a risk prediction model for severe pregnancy complications in hypertensive disorders of pregnancy: (1) Serious fetal malformation/abnormality; (2) Severe mental disorders, unable to express their wishes; (3) There are obvious other abnormal signs, laboratory examinations and other clinical diseases, and according to the judgment of the investigator, they are not suitable to participate in the researcher; (4) According to the investigator's judgment, it is impossible to observe and follow-up to obtain delivery information.

Design outcomes

Primary

MeasureTime frame
Arachidonic acid inhibition rate;Placental growth factor;Mean arterial pressure;Uterine arterial pulse index;

Secondary

MeasureTime frame
S/D ratio of umbilical artery;Umbilical artery pulsatility index;Pregnancy associated plasma protein-A;Armor embryo protein;Human Chorionic Gonadotropin;Progesterone;Free estriol;

Countries

China

Contacts

Public ContactLi Baohua

Women's Hospital, School of Medicine, Zhejiang University

lbh19787@zju.edu.cn+86 13777477364

Outcome results

None listed

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