Actively Recruiting
The Project of Gestational Hypertension and Preeclampsia Screening and Prevention Center
Led by The Third Affiliated Hospital of Guangzhou Medical University · Updated on 2024-09-19
50000
Participants Needed
1
Research Sites
282 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Preeclampsia is the main cause of illness and death in pregnant women and fetuses. Currently, there is no effective treatment for preeclampsia in clinical practice, and the fundamental treatment is still termination of pregnancy and placental delivery. Therefore, early prediction of preeclampsia and targeted strengthening of high-risk pregnant women supervision, early intervention and diagnosis and treatment can greatly reduce the serious obstetric complications and perinatal maternal and fetal deaths caused by preeclampsia, which has significant social and clinical significance.
CONDITIONS
Official Title
The Project of Gestational Hypertension and Preeclampsia Screening and Prevention Center
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Pregnant women screened for preeclampsia risk using clinical risk factors listed in NICE guidelines (2019)
- Pregnant women assessed in the first trimester using maternal factors plus MAP and PLGF with or without UtA-PI, or in the second and third trimesters using PLGF or sFlt-1/PLGF
- Voluntary participation and signing of informed consent
You will not qualify if you...
- Severe fetal malformation or no fetal heartbeat
- Regular use of aspirin before joining the study
- Presence of other significant abnormal signs, laboratory test results, or clinical diseases deemed unsuitable by researchers
- Inability to provide follow-up and delivery information
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
FANG HE
Guangzhou, Guangdong, China, 510150
Actively Recruiting
Research Team
D
Dunjin Chen, Professor
CONTACT
F
Fang He, M.D
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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