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首页 临床进展 Randomized Evaluative Study of Phenylephrine Or Norepinephrine for maintenance of blood pressure during spinal anaesthesia for caesarean Delivery: The RESPOND study

【ChiCTR-TRC-12002135】Randomized Evaluative Study of Phenylephrine Or Norepinephrine for maintenance of blood pressure during spinal anaesthesia for caesarean Delivery: The RESPOND study

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基本信息
登记号

ChiCTR-TRC-12002135

试验状态

结束

药物名称

/

药物类型

/

规范名称

/

首次公示信息日的期

2012-04-29

临床申请受理号

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靶点

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适应症

Pregnancy

试验通俗题目

Randomized Evaluative Study of Phenylephrine Or Norepinephrine for maintenance of blood pressure during spinal anaesthesia for caesarean Delivery: The RESPOND study

试验专业题目

Randomized Evaluative Study of Phenylephrine Or Norepinephrine for maintenance of blood pressure during spinal anaesthesia for caesarean Delivery: The RESPOND study

申办单位信息
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申请人名称
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联系人邮箱
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联系人邮编

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临床试验信息
试验目的

Study of Phenylephrine Or Norepinephrine for maintenance of blood pressure during spinal anaesthesia for caesarean Delivery

试验分类
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试验类型

随机平行对照

试验分期

Ⅳ期

随机化

RCT

盲法

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试验项目经费来源

RGC GRF

试验范围

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目标入组人数

104

实际入组人数

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第一例入组时间

2012-07-01

试验终止时间

1990-01-01

是否属于一致性

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入选标准

American Society of Anesthesiologists Physical Status 1 or 2 normotensive non-labouring parturients with term singleton pregnancies who are scheduled for elective Caesarean section and who have been judged suitable and have agreed to have for spinal anaesthesia according to usual clinical criteria.；

排除标准

Known fetal abnormality, preexisting or pregnancy-induced hypertension, known cardiovascular or cerebrovascular disease, thrombocytopaenia, coagulopathy, or any medical contraindication to spinal anaesthesia, weight <50 kg or >100 kg, height <140 cm or >180 cm, inability or refusal to give informed consent, age < 18 years, patients taking monoamine oxidase inhibitors or tricyclic antidepressants, patients with mesenteric or peripheral vascular thrombosis, patients with renal impairment.；

研究者信息
研究负责人姓名
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试验机构

Prince of Wales Hospital, The Chinese University of Hong Kong

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