Basic and Clinical Research of Pregnancy-Induced Hypertension
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: no Intervention.
- Who it may be relevant to
- Registry conditions: Pregnancy-induced Hypertension. Basic parameters: 20 years — 50 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- China
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Collect Blood Pressure, Blood, Amniotic Fluid, Placenta and Other Samples From Normal Pregnant Women, Patients With Pregnancy-induced Hypertension and Those Who Have Experienced Miscarriage, and Conduct Tests on Them.
Overview
Collect blood pressure, blood, amniotic fluid, placenta and other samples from normal pregnant women, patients with pregnancy-induced hypertension and those who have experienced miscarriage, and conduct tests on them.
Interventions
- Other no Intervention
observation
Primary outcome measures
- PIH [Time frame: Early pregnancy：Weeks 1 to 12 (the first to third months of pregnancy) ；mid-pregnancy：Weeks 13 to 27 (the 4th to 6th month of pregnancy) ；post-delivery period：Weeks 28 to 40 (the 7th to 9th months of pregnancy)；the day of delivery。]
Secondary outcome measures (3)
- PIH [Time frame: delivery]
- PIH [Time frame: delivery]
- PIH [Time frame: delivery]
Eligibility criteria
Inclusion criteria
\- Healthy pregnant women, patients with miscarriage, etc.
Exclusion criteria
- Heart disease, infections, etc. in pregnant women Uncooperative patients
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Observational model
- Cohort
Study locations
China · 1 center
- The Second Affiliated Hospital of Wenzhou Medical University — Wenzhou
Identifiers
NCT: NCT07464379 · SAHoWMU-CR2025-03-134