跳至主要内容
临床试验/EUCTR2012-005770-57-SE
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

发起方
department of OBstetrics, Sahlgrenska university hospital

相似试验