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临床试验/NCT05836610
NCT05836610招募中4 期

Hydrocortisone Therapy Optimization During Hypothermia Treatment in Asphyxiated Neonates - a Pharmacokinetic Study

Semmelweis University2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2021年9月21日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
招募中
入组人数
50
试验地点
2
主要终点
Mean blood pressure increase

研究概览

简要总结

This is a prospective, single center, pharmacokinetic study of intravenous hydrocortisone therapy for systemic low blood pressure during hypothermia treatment in asphyxiated newborns. Patients will be allocated to hydrocortisone supplementation while receiving conventional inotropic therapy as needed.

The hypothesis is that a detailed study of hydrocortisone pharmacokinetics during therapeutic hypothermia would help to personalize steroid supplementation in asphyxiated neonates. As the overall metabolic rate decreases with lower body temperature, drug metabolism is likely to be reduced as well, and lower doses, or less frequent dosing will be sufficient to achieve the targeted steroid range and biological effects in asphyxiated neonates with relative adrenal insufficiency. Thus, the investigators are planning to measure initial, baseline serum cortisol levels and serial serum cortisol levels after hydrocortisone supplementation in cooled asphyxiated neonates.

详细描述

The ultimate goal of the present study, is to describe a new approach of more personalized and safe care to infants with birth asphyxia and hemodynamic instability.

Asphyxiated infants often present with multiorgan failure and low blood pressure. Therapeutic hypothermia, the standard of care, could worsen hemodynamic instability; therefore, treatment of cardiovascular impairment represents a major challenge in this clinical setting. An association was previously described between hypotension and low serum cortisol values in this patient population, and it was suggested that relative adrenal insufficiency (RAI) is an important factor in the circulatory compromise of these patients. In the "CORTISoL" clinical trial, it was also demonstrated that low-dose hydrocortisone therapy was effective in the treatment of cardiovascular impairment in asphyxiated neonates; however, some gaps remain in the knowledge on optimal dosing. Importantly, steroid therapy should be administered at the lowest effective dose and for the shortest possible duration in this vulnerable population.

In the current pharmacokinetic study, the investigators propose a stepwise approach to more detailed understanding of RAI and hydrocortisone pharmacokinetics in asphyxiated neonates. The findings would certainly aid clinical decision-making and allow for more personalized therapeutic interventions for the treatment of hemodynamic instability.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Sequential
主要目的
Treatment
盲法
None

入排标准

年龄范围
— 至 72 Hours(Child)
性别
All
接受健康志愿者

入选标准

  • gestational age ≥ 36 weeks
  • provision of whole-body hypothermia treatment (as described by Azzopardi et al.)
  • presence of systemic hypotension (defined as a mean arterial pressure less than the gestational age in weeks)
  • indication for hydrocortisone treatment during hypothermia by the attending physician
  • indwelling arterial catheter to take blood samples without additional painful punctures: umbilical arterial catheter or peripheral arterial catheter
  • written informed parental consent

排除标准

  • infants who are expected to be > 6 hours of age (not suitable for cooling)
  • critical congenital abnormalities
  • genetic disease
  • signed informed consent is unavailable

研究组 & 干预措施

Modified dose hydrocortisone

Active Comparator

The modified dose of hydrocortisone therapy will be determined based on the pharmacokinetic results.

干预措施: Hydrocortisone (Drug)

Standard dose hydrocortisone

Active Comparator

The standard dose of hydrocortisone therapy in neonates for hypotension is 0.5 mg/kg every 6 hours.

干预措施: Hydrocortisone (Drug)

结局指标

主要结局

Mean blood pressure increase

时间窗: 2 hours

5 mmHg increase in mean arterial blood pressure after drug administration

次要结局

  • Presence of relative adrenal insufficiency at baseline(Before hydrocortisone administration within max. 72 hours)
  • Long term neurodevelopmental outcome(18-42 month)
  • Cardiovascular management(72 hours)
  • MRI outcome(4-10 days)

研究者

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

Kata Kovacs

Assistant lecturer

Semmelweis University

研究点 (2)

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