Obstetric and Perinatal Outcomes of Women With COVID-19 (GROCO)
Obstetric and Perinatal Outcomes of Women With COVID-19: A Prospective Cohort Study
研究概览
详细说明
Clinical manifestations of COVID-19 can range from a benign upper respiratory tract infection to severe acute respiratory distress syndrome (ARDS), fatal in 1% of cases. However, pregnant women and their fetuses could particularly be vulnerable to the infection, as shown by previous human coronavirus outbreaks (SARS-CoV and MERS-CoV).
Cases will be recruited among all pregnant women aged >18 years old who have tested positive for COVID-19 and are followed in a maternity belonging to the French South Regional Perinatology Network. Voluntary physicians will refer eligible participants to the study-coordinating center at APHM University Hospital. The participants will be followed by phone after having provided an informed consent. Clinical symptoms, laboratory and imaging findings, maternal and perinatal outcomes will be recorded.
研究类型
注册 (实际的)
联系人和位置
学习地点
-
-
Paca
-
Marseille、Paca、法国、13354
- Assistance Publique Hôpitaux de Marseille
-
-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
取样方法
研究人群
描述
Inclusion Criteria:
- Pregnant women
- Able to give informed consent
- Diagnosed with COVID-19
Exclusion Criteria:
- Patients Refusing to Participate in the Study
- Patients who do not speak French well enough to benefit from clear and intelligible information
学习计划
研究是如何设计的?
设计细节
队列和干预
团体/队列 |
干预/治疗 |
|---|---|
|
pregnant women with COVID-19
Pregnant women who have tested positive for COVID-19
|
clinical data collection
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Compare the complications rates
大体时间:12 months
|
To compare the complications rates of pregnant women tested positive for the SARS-CoV-2 (study group), with reference rates in a Covid-free population.
|
12 months
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Clinical presentation
大体时间:12 months
|
To record clinical presentation of pregnant participants with COVID-19 by questionnaire and clinical evaluation
|
12 months
|
合作者和调查者
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他研究编号
- 2020-18
- ID RCB (其他标识符:2026-A01760-51)
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
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