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RECRUITINGPhase 4INTERVENTIONAL

Hydrocortisone Therapy Optimization During Hypothermia Treatment in Asphyxiated Neonates

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

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

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.

Who May Be Eligible (Plain English)

Who May Qualify: - 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 Who Should NOT Join This Trial: - infants who are expected to be \> 6 hours of age (not suitable for cooling) - critical congenital abnormalities - genetic disease - signed willing to sign a consent form is unavailable Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * 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 Exclusion Criteria: * infants who are expected to be \> 6 hours of age (not suitable for cooling) * critical congenital abnormalities * genetic disease * signed informed consent is unavailable

Treatments Being Tested

DRUG

Hydrocortisone

intravenous bolus hydrocortisone therapy during hypothermia treatment

Locations (1)

Semmelweis University Department of Pediatrics (Bókay street Unit)
Budapest, Pest County, Hungary