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临床试验/NCT04373902
NCT04373902进行中(未招募)不适用

Physiological-based Cord Clamping Versus Immediate Cord Clamping for Infants Born With Congenital Diaphragmatic Hernia: a Multicentre, Randomised Controlled Trial

Erasmus Medical Center9 个研究点 分布在 7 个国家目标入组 140 人开始时间: 2020年5月11日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
140
试验地点
9
主要终点
Number of participants with pulmonary hypertension diagnosed in the first 24 hours after birth.

研究概览

简要总结

Pulmonary hypertension is a major determinant of postnatal survival in infants with a congenital diaphragmatic hernia (CDH). The current care during the perinatal stabilisation period in infants born with this rare birth defect might contribute to the development of pulmonary hypertension after birth - in particular umbilical cord clamping before lung aeration. An ovine model of diaphragmatic hernia demonstrated that cord clamping after lung aeration, called physiological-based cord clamping (PBCC), avoided the initial high pressures in the lung vasculature while maintaining adequate blood flow, thereby avoiding vascular remodelling and aggravation of pulmonary hypertension. The investigators aim to investigate if the implementation of PBCC in the perinatal stabilisation period of infants born with a CDH could reduce the incidence of pulmonary hypertension in the first 24 hours after birth.

The investigators will perform a multicentre, randomised controlled trial in infants with an isolated CDH. Before birth, infants will be randomised to either PBCC or immediate cord clamping, stratified by treatment centre and severity of pulmonary hypoplasia on antenatal ultrasound. For performing PBCC a purpose-designed resuscitation module (the Concord Birth Trolley) will be used.

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
None

入排标准

年龄范围
35 Weeks 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Left-sided CDH
  • Isolated CDH: no associated structural or genetic abnormalities that are diagnosed before birth
  • Gestational age at delivery ≥35.0 weeks
  • Parental written informed consent

排除标准

  • Right-sided or bilateral CDH
  • Gestational age at delivery <35.0 weeks
  • Maternal contraindications: anterior placenta praevia, placental abruption
  • High urgency caesarean section, with intended interval to delivery <15 min
  • Cases that have been treated during pregnancy with experimental drug therapy aiming to decrease the occurrence of pulmonary hypertension
  • Twin pregnancies in which the infant diagnosed with a CDH is born first
  • Multiple birth >2 (triplets or higher order)

结局指标

主要结局

Number of participants with pulmonary hypertension diagnosed in the first 24 hours after birth.

时间窗: First 24 hours after birth

Pulmonary hypertension is present if at least 2 of the following 4 criteria are present or if the infant requires extracorporeal membrane oxygenation (ECMO) in the first 24 hours after birth: 1. Right ventricular systolic pressure (RVSP) ≥2/3 systemic systolic pressure\* 2. Right ventricle (RV) dilatation/septal displacement or RV dysfunction +/- left ventricle (LV) dysfunction\* 3. Pre-post ductal SpO2 difference \>10% for at least 15 consecutive minutes 4. Oxygenation Index \>20\*\* \*as found on first ultrasound in first 24 hours after birth; \*\*highest value measured in first 24 hours after birth The following echocardiographic parameters will be collected to objectify these criteria: * RV size * Pulmonary artery acceleration time (PAAT), right ventricular ejection time (RVET), PAAT:RVET ratio * Intraventricular septum configuration * LV systolic eccentricity index * Mean airway pressure * PaO2 * FiO2 * Preductal+postductal SpO2

次要结局

  • Neonatal: presence of 3 or more criteria for pulmonary hypertension or extracorporeal membrane oxygenation within 24 hours after birth(The first 24 hours after delivery)
  • Neonatal: number of patients requiring ECMO therapy(From admission to the ICU until the date of death or the date of discharge home, whichever came first)
  • Neonatal: number of days of duration of mechanical ventilation(From admission to the ICU until the date of discharge to another ward or home, whichever came first,through study completion an average of one year)
  • Neonatal: duration of admission to the tertiary care hospital(From admission to the ICU until the date of discharge to another ward or home, whichever came first)
  • Neonatal: number of days of duration of supplemental oxygen need(From admission to the ICU until the date of discharge to another ward or home, whichever came first,through study completion an average of one year)
  • Maternal: number of patients with postpartum haemorrhage(The first 24 hours after delivery)
  • Neonatal: mortality before discharge from the tertiary care hospital(From birth till discharge from the tertiary care hospital, through study completion an average of one year)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Philip L.J. DeKoninck

Principal Investigator, Dr.

Erasmus Medical Center

研究点 (9)

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