EUCTR2005-000289-38-DK进行中（未招募）不适用
acetylcystein til gravide med præeklampsi
Organisation name was not entered0 个研究点目标入组 30 人开始时间: 2005年4月5日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 30
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
- •Alder>18 år. Tidligere normotensiv kvinde, som efter 20. graviditetsuge, ved to blodtryksmålinger (4 timers mellemrum) har >90 i diastolisk blodtryk og proteinuri >300 mg/l eller ++ på dipstix (2 målinger med 4 timers mellemrum). Desuden skal kvinden have underskrevet informeret samtykke og gerne fuldmagt.
- •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
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Sygdom bortset fra præeklampsi, der kræver medicinsk behandling(heri også antibiotisk- og AK-behandling).
- •Ved antibiotikabahandling pga truende præmatur fødsel kan kvinden indgå. Forsøgsmedicin tages to timer forskudt fra antibiotika.
- •Ved p.n. medicinering af astma og allergi kan patienten fortsat indgå i projektet.
- •Allergi overfor indholdstofferne. Arvelig galactose intolerans (Lapp Lactase Deficiency) eller glucose/galactosemalabsorbtion.
研究者
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