EUCTR2007-005269-36-IT进行中（未招募）不适用
INTRATHECAL ROPIVACAINE USE IN CESAREAN SECTION : DETERMINATION OF ?MINIMUM LOCAL ANESTHETIC DOSE (MLAD)? - OST 02/08
AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI0 个研究点开始时间: 2007年10月12日最近更新:
适应症
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
- •Gathering of informed consent;
- •Age between 18 and 40 years
- •Maternal height between 150 and 190 cm,
- •Maternal weight between 50 and 120 kg,
- •Women who underwent elective or scheduled cesarean section.
- •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
- •Obstetrical complications associated with a higher hemorrhagic risk (e.g. central placenta praevia),
- •Twin or multiple pregnancies,
- •Inherited or acquired coagulation disorders,
- •Skin infections or previous/actual spinal disorders,
- •Urgent cesarean section,
- •Severe clinical conditions that do not allow the enrollment of the patient,
- •Use of experimental drugs within months before the inclusion in the study
研究者
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