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临床试验/NCT04789005
NCT04789005已完成3 期

Comparison of Intravenous Phenylephrine and Norepinephrine for Treatment of Spinal-induced Hypotension in Caesarian Deliveries

Tribhuvan University Teaching Hospital, Institute Of Medicine.1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2019年11月10日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
80
试验地点
1
主要终点
compare percentage of incidence of bradycardia between the two groups

研究概览

简要总结

Hypotension after spinal anaesthesia for cesarean deliveries is frequently encountered. Phenylephrine an α-agonist is commonly used for the prevention and treatment of spinal-induced hypotension. Phenylephrine causes baroreceptor-mediated bradycardia leading to subsequent reduction in cardiac output. Preservation of heart rate and cardiac output is important in high-risk conditions such as placental insufficiency, fetal distress and maternal cardiac disease. Recently, norepinephrine has been found as effective as phenylephrine in treatment of spinal induced hypotension. When norepinephrine is used as a bolus, it is effective at maintaining blood pressure while also conferring a greater heart rate and cardiac output compared to phenylephrine.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Elective cesarean delivery under spinal anaesthesia ASA PS II Age ≥18 years Singleton pregnancy beyond 37 weeks' gestation Weight between 50 and 100 kg Height between 150 and 180 cm

排除标准

  • Patient refusal to participate Allergy or hypersensitivity to Norepinephrine or Phenylephrine Preexisting or pregnancy-induced hypertension Cardiovascular or cerebrovascular disease Fetal abnormalities Use of monoamine oxidase inhibitors or tricyclic antidepressants

研究组 & 干预措施

Phenylephrine group

Active Comparator

Phenylephrine 100mcg was administered manually by the anaesthesiologist every time the SBP was 20% lower than baseline and the HR ≥60 bpm.

干预措施: Phenylephrine (Drug)

Norepinephrine group

Experimental

Norepinephrine 8mcg was administered manually by the anaesthesiologist every time the SBP was 20% lower than baseline and the HR ≥60 bpm.

干预措施: Norepinephrine (Drug)

结局指标

主要结局

compare percentage of incidence of bradycardia between the two groups

时间窗: 6 months

To compare percentage of incidence of hypotension between two groups.

时间窗: 6 months

To compare blood pressure between two groups.

时间窗: 6 months

次要结局

未报告次要终点

研究者

发起方
Tribhuvan University Teaching Hospital, Institute Of Medicine.
申办方类型
Other
责任方
Principal Investigator
主要研究者

ALLEN SUWAL

Resident Anaesthesiology

Tribhuvan University Teaching Hospital, Institute Of Medicine.

研究点 (1)

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