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临床试验/NCT05279703
NCT05279703Unknown4 期

The Use of Epinephrine Infusion for Prophylaxis Against Maternal Hypotension During Cesarean Delivery: a Randomized Controlled Dose-finding Trial

Kasr El Aini Hospital1 个研究点 分布在 1 个国家目标入组 276 人开始时间: 2022年3月21日最近更新:
适应症
干预措施

试验速览

阶段
4 期
发起方
入组人数
276
试验地点
1
主要终点
incidence of postspinal hypotension

研究概览

简要总结

Maternal hypotension after spinal block is a common complication after subarachnoid block in this population. The incidence of maternal hypotension is nearly 60% when prophylactic vasopressors are not used. Therefore, it is highly recommended to use vasopressors, preferably as continuous infusion, for prophylaxis rather than delaying their use until hypotension occurs.

Phenylephrine (PE) is the recommended drug for prophylaxis against hypotension during cesarean delivery; however, the use of PE is commonly associated with decreased heart rate and probably cardiac output because PE is a pure alpha adrenoreceptor agonist. Introduction of NE in obstetric practice had shown favorable maternal and neonatal outcomes and was associated with higher heart rate and cardiac output compared to PE. However, there is still some mothers who develop bradycardia and diminished cardiac output with the use of NE. The most desired scenario during hemodynamic management of mothers during cesarean delivery would achieve the least possible incidences of maternal hypotension, bradycardia and reactive hypertension. Therefore, it is warranted to reach a vasopressor regimen with the most stable hemodynamic profile.

In the last year, epinephrine was reported for the first time in obstetric practice with acceptable safety on the mother and the fetus. However, there is still lack of data about the most appropriate dose for infusion during cesarean delivery. This study aims to compare three prophylactic infusion rates for epinephrine during cesarean delivery.

详细描述

Upon arrival to the operating room, the patient will be in supine position with left uterine displacement using a wedge below the right buttock. Routine monitoring will be applied (electrocardiography, pulse oximetry, and non-invasive blood pressure monitor). An 18G-cannula will be inserted, and the patients will receive 10 mg metoclopramide. Baseline heart rate and systolic blood pressure will be recorded as the average of three consecutive readings with 2-minutes interval.

Lactated Ringer's solution will be infused at rate of 15 mL/Kg over 10 minutes as a co-load; spinal anesthesia will be achieved by injecting 10 mg of hyperbaric bupivacaine and 20 mcg fentanyl into the subarachnoid space at L3-L4 or L4-L5 interspace using 25G spinal needle.

After subarachnoid block, mothers will be placed in supine position with left-lateral tilt and the vasopressor infusion will be started.

  • 0.01 mcg group
  • 0.02 mcg group
  • 0.03 mcg group The vasopressor infusion will be through the same line as the fluid a three-way stopcock. The vasopressor infusion will be stopped if heart rate became ≥130% of baseline or systolic blood pressure ≥120% of baseline, otherwise the infusion will be stopped 5 minutes after delivery of the baby.

Block success will be assessed after 5 minutes from intrathecal injection of local anesthetic; and will be confirmed if sensory block level is at T4.

研究设计

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

入排标准

年龄范围
18 Years 至 40 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • full-term singleton pregnant women
  • American society of anesthesiologist-physical status I or II,
  • scheduled for elective cesarean delivery

排除标准

  • Patients with uncontrolled cardiac morbidities (patients with tight valvular lesion, impaired contractility with ejection fraction < 50%, heart block, and arrhythmias),
  • hypertensive disorders of pregnancy,
  • peripartum bleeding,
  • coagulation disorders (patients with INR >1.4 and or platelet count < 80000 /dL) or
  • any contraindication to regional anesthesia,
  • and baseline systolic blood pressure (SBP) < 100 mmHg

研究组 & 干预措施

0.03 mcg group

Active Comparator

epinephrine infusion will be started after subarachnoid block until 5 minutes after delivery of the baby

干预措施: Epinephrine 0.03 (Drug)

0.02 mcg group

Active Comparator

epinephrine infusion will be started after subarachnoid block until 5 minutes after delivery of the baby

干预措施: Epinephrin 0.02 (Drug)

0.01 mcg group

Active Comparator

epinephrine infusion will be started after subarachnoid block until 5 minutes after delivery of the baby

干预措施: Epinephrin 0.01 (Drug)

结局指标

主要结局

incidence of postspinal hypotension

时间窗: 1 minute after subarachnoid injection till 5 minutes after baby delivery

systolic blood pressure ≤80% of the baseline reading

次要结局

  • incidence of tachycardia(1 minute after subarachnoid injection till 5 minutes after baby delivery)
  • mean systolic blood pressure(1 minute after subarachnoid injection, every 2 minutes during procedure, till 5 minutes after baby delivery)
  • total ephedrine requirement(1 minute after subarachnoid injection till 5 minutes after baby delivery)
  • umbilical blood pH(5 minutes after delivery)
  • incidence of severe hypotension(1 minute after subarachnoid injection till 5 minutes after baby delivery)
  • total atropine requirement(1 minute after subarachnoid injection till 5 minutes after baby delivery)
  • Apgar score(5 minutes after delivery)
  • umbilical blood PO2(5 minutes after delivery)
  • incidence of hypertension(1 minute after subarachnoid injection till 5 minutes after baby delivery)
  • mean heart rate(1 minute after subarachnoid injection, every 2 minutes during procedure, till 5 minutes after baby delivery)
  • umbilical blood PCO2(5 minutes after delivery)
  • umbilical blood HCO3(5 minutes after delivery)

研究者

发起方
Kasr El Aini Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Maha Mostafa Ahmad, MD

Principal Investigator

Kasr El Aini Hospital

研究点 (1)

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