EUCTR2021-006632-67-FR进行中（未招募）1 期
Alkalinization of adrenalized lidocaine in extending epidural analgesia for extremely urgent cesarean section during labor: a randomized controlled trial. - QETA
CHU de Bordeaux0 个研究点目标入组 66 人开始时间: 2022年1月31日最近更新:
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相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 66
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
- •- Adult patients,
- •- Affiliated to social security
- •- Informed consent signed by the participant and the investigating physician at the latest after the therapeutic intervention
- •- Initial indication for vaginal delivery
- •- Benefiting from emergency caesarean section during labour for fetal extraction with a maximum 15-minute decision-to-delivery delay (i.e. code red Caesarean 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 66
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •- Opposition to participation in research before delivery
- •- Refusal or impossibility of informed consent
- •- Lack of understanding or significant language barrier
- •- Initial indication for general anaesthesia defined by the following situations: non-functional epidural analgesia, altered consciousness, eclampsia, suspicion of amniotic embolism, confirmed or suspected severe haemorrhage occurring before birth
- •- Contraindication to the use of the products defined in the protocol : lidocaïne
- •- Persons placed under judicial protection
研究者
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