EUCTR2012-005770-57-SE进行中(未招募)不适用
Clinical effect of Atenativ treatment on uterine blood flow and the amount of Atenativ needed to maintain a normal antithrombin level during two weeks in early and severe preeclampsia
department of OBstetrics, Sahlgrenska university hospital0 个研究点开始时间: 2012年12月27日最近更新:
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- Female
入选标准
- •Women with severe early-onset preeclampsia during gestational week 23-29+0.
- •2. Severe preeclampsia as defined by international criteria (1,2)
- •Blood pressure >160/110 mmHg (measured twice 30 minutes apart).
- •proteinuria (>5 .0 g/L per 24 hours or >3 + labstick in at least two random
- •samples six hours apart) after 20th gestational week.
- •Blood pressure >140/90 mmHg and proteinuria >5.0 g/24 h.
- •preeclampsia ( blood pressure > 140/90 and proteinuria >0.3 g/24 h) with IUGR or subjective symptoms as epigastic pain (HELLP), headache, dizziness or visual disturbancies, oligouri < 600 ml/24 h, coagulation disturbancies.
- •3. AT level <0.8 kIE/LC
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 6
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •1.History of congenital AT deficiency
- •2.Severe preeclampsia with demand on acute delivery within 24 hours according to the investigators judgement
- •3.Concomitant administration of anticoagulants and platelet inhibitors within 2 weeks
- •4.Chronic renal disease
- •5.Diabetes melittus or gestational diabetes
- •6.Intrauterine fetal death
- •7.Participation in another clinical study
- •8. Multiple pregnancies
研究者
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