ISRCTN13060768进行中（未招募）未知
Investigating organ complications in preeclampsia during and after pregnancy and the pregnant woman's and partner's health in the postpartum period: An observational cohort study involving the GO PROVE - Gothenburg Preeclampsia Obstetric Adverse Events and UPMOST - Uppsala Pregnancy Complication Study
Sahlgrenska University Hospital0 个研究点目标入组 300 人开始时间: 2020年7月27日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 300
研究概览
简要总结
2021 Protocol article in https://pubmed.ncbi.nlm.nih.gov/34819281/ (added 26/11/2021) 2023 Results article in https://pubmed.ncbi.nlm.nih.gov/37080010/ (added 17/08/2023)
研究设计
- 研究类型
- Observational
入排标准
- 性别
- Female
入选标准
- •Preeclampsia cohort:
- •1. Primiparous and parous pregnant women
- •2. Aged =18 years
- •3. Diagnosis of preeclampsia after gestational week 20
- •Control cohort:
- •1. Primiparous and parous women
- •2. Aged =18 years
- •3. Healthy pregnancies matched for gestational age
排除标准
- •Current participant exclusion criteria as of 10/01/2022:
- •1. Unable to give written informed consent
- •2. Magnetic resonance imaging (MRI) contraindications, including claustrophobia, for MR group only
- •3. Diabetes Mellitus before or during pregnancy, pre-existing cardiovascular, renal, or cerebral disease, or pre-existing hypertension for special investigations including MRI, echocardiography, cerebral doppler measurements, and cognitive function assessment
- •Previous participant exclusion criteria:
- •1. Unable to give written informed consent
- •2. Pre-existing hypertension
- •3. Diabetes Mellitus before or during pregnancy
- •4. Pre-existing cardiovascular, renal, or cerebral disease
- •5. Magnetic resonance imaging (MRI) contraindications, including claustrophobia, for MR group only
研究者
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