Clinical Trials Directory

Trials / Completed

CompletedNCT00817401

Systemic Hypothermia Improves Outcome of Hypoxic-Ischemic Encephalopathy

Effect of Systemic Hypothermia on Neonatal Hypoxic-Ischemic Encephalopathy

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
100 (actual)
Sponsor
Zhengzhou University · Academic / Other
Sex
All
Age
1 Hour – 10 Hours
Healthy volunteers
Not accepted

Summary

Perinatal asphyxia-induced brain injury is one of the most common causes of morbidity and mortality in term and preterm neonates. Birth asphyxia accounts for 23% of neonatal deaths globally and survivors suffer from long term neurological disability and impairment. Although many neuroprotective strategies appeared promising in animal models, most of them were not feasible and effective in human newborns. However, hypothermia was reported not to be effective if introduced beyond and thus should be introduced within 6 hrs after birth.Applying this selection criterion naturally would deprive many patients of the opportunity of hypothermia treatment.

Detailed description

Hypoxic-ischemic encephalopathy of the newborn infant remains a significant socio-economic health problem worldwide. Moderate to severe HIE of newborn infants is associated with a high rate of death or long-term disabilities. Historically, treatment has been purely supportive including stabilizing cardio-respiratory functions and treating convulsions. Recent multi-center trials assessing the effects of hypothermia demonstrated improved outcome in term neonates with moderate hypoxic-ischemic encephalopathy (HIE). However, hypothermia was not effective beyond 6 hrs after brain injury. The aim of this study was to investigate whether systemic hypothermia induced up to 10 hrs after birth would improve the neurodevelopmental outcome at 18 months in infants with moderate or severe HIE.

Conditions

Interventions

TypeNameDescription
DEVICEhypothermiaFor the systemic hypothermia treatment (TS Med 200, Germany), the infants were nursed under an open unit, covered only by a diaper and a thin linen, loosing heat to the environment and to a cooling mat¬tress which was perfused by circulating liquid at a variable temperature. The rectal temperature was targeted at 33.5 °C (range of 33 to 34 °C) and was meant to be achieved within 60 min. The body temperature was checked every 10 min during induction hypothermia and every hour during the remaining period of cooling. The duration of hypothermia was 72 hrs. Rewarming was started by stopping the cooling system. The infant was meant to reach a 36.5°C rectal temperature in 6 hrs after stopping cooling to prevent rebound hyperthermia.

Timeline

Start date
2002-07-01
Primary completion
2008-06-01
Completion
2008-06-01
First posted
2009-01-06
Last updated
2009-01-06

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT00817401. Inclusion in this directory is not an endorsement.