CTIS2022-500933-10-00招募中1 期
Aspirin for the Prevention of Preeclampsia and Pregnancy outcomes in nulliparous women after Assisted Reproductive Technology.APPART trial - RC31/21/0337
适应症
试验速览
- 阶段
- 1 期
- 状态
- 招募中
- 入组人数
- 1,164
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 64（—）
入选标准
- •Nulliparous women aged 18 years or more, Pregnancy following ART, including in vitro fertilization (IVF), intracytoplasmic sperm injection (ICSI), oocyte donation or intrauterine insemination with sperm donor, Singleton pregnancy, Evolutive pregnancy between 9 and 14 weeks of gestation, Women affiliated to a French Social Security Insurance or equivalent social protection, Written informed consent
排除标准
- •Major fetal abnormality, Regular treatment with aspirin (including antiphospholipid syndrome), Aspirin contraindications (allergy, von Willebrand disease, peptic ulceration, hemophilia), Women protected by law., Women included in another interventional study.
研究者
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