EUCTR2007-005231-28-AT进行中（未招募）不适用
Postoperative Analgesie and Antihyperalgesia of Tramadol and Acetaminophen peroral after Caesarean Section - Tramalstudie
Med. Univ. Wien, Universitätsklinik für Anästhesie, allgemeine Intensivmedizin und Schmerzmedizin0 个研究点目标入组 120 人开始时间: 2008年8月28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
- 入组人数
- 120
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
- •Female patients between 18 and 45 years, ASA-Status 1-2, BMI 19-29, that are scheduled for planned caesarean section and have given written informed consent, will be included
- •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
- •Exclusion criteria are known allergies or hypersensitivities to evaluated drugs, history of pain syndrome, substance abuse, preeclampsia or eclampsia, deviation from standardised surgical procedure, treatment with magnesium sulfate, renal or hepatic impairment and deviations from the standardized anaesthetic treatment.
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