CoolCap Trial, Treatment of Perinatal Hypoxic-Ischemic Encephalopathy

This study has been completed.
Sponsor:
Information provided by:
Olympic Medical
ClinicalTrials.gov Identifier:
NCT00383305
First received: September 29, 2006
Last updated: NA
Last verified: September 2006
History: No changes posted

September 29, 2006
September 29, 2006
July 1999
Not Provided
Combined death or severe neurodevelopmental disability in the first 18 months of life.
Same as current
No Changes Posted
  • Length of hospitalization during NICU course in those surviving to discharge and for whom support was not withdrawn.
  • Multi-organ dysfunction (3 or more organ systems) in the neonatal period.
  • Rate of multiple handicap in survivors (Multiple handicap will be defined as the presence of any two of the following in an infant: neuromotor disability (Level 3-5 on GMF classification), mental delay, epilepsy, cortical visual impairment, sensorineural
  • Bayley PDI score
  • Sensorineural hearing loss >= 40 dB
  • Epilepsy: recurrent seizures beyond the neonatal period, requiring anticonvulsant therapy at the time of assessment.
  • Microcephaly: head circumference < (mean - 2SD)
Same as current
Not Provided
Not Provided
 
CoolCap Trial, Treatment of Perinatal Hypoxic-Ischemic Encephalopathy
Brain-Cooling for the Treatment of Perinatal Hypoxic-Ischemic Encephalopathy

This is a research study of head cooling. Its goal is to determine whether cooling babies' heads can reduce or prevent brain damage that may have resulted from temporarily reduced oxygen supply to the brain. In this study, half of the babies (selected at random) will have a special cooling cap with circulating water placed on their head for 72 hours to lower the temperature of their brain. The rest of the baby's body will be maintained at a defined temperature by a standard overhead radiant heater. The study protocol includes the taking and analysis of blood samples, performance of brain wave tests, imaging of the brain by ultrasound, and other tests as clinically indicated. Neurodevelopmental outcome will also be assessed at 18 months of age.

The objective of this study is to determine whether head cooling with mild systemic hypothermia in term infants following perinatal asphyxia is a safe procedure that improves survival without neurodevelopmental disability. Outcome will be assessed by survival and neurological and neurodevelopmental testing at 18 months of age.

Within 6 hours of birth, infants will be randomized to either a non-cooled control group with rectal temperature kept at 37+/-0.5 degC or to head cooling with mild systemic hypothermia as follows. A cooling device capable of circulating cool water in a temperature-regulated manner through a cap fitted around the infant's scalp will cool the head. The core rectal temperature of the infant will be maintained at 34.5+/-0.5 degC by adjusting the cap water temperature. The infant's rectal, nasopharyngeal, scalp (fontanel), and skin (abdominal) temperatures will be continuously monitored. Also, metabolic, cardiovascular, pulmonary and coagulation laboratory measurements will be assessed at predefined time points. Cooling will be maintained for 72 hours, followed by four hours of rewarming, with the goal of raising the rectal temperature to normal body temperature by 0.5 degC per hour. The outcome measure of severe neurodevelopmental disability and survival rates at 18 months of age will be assessed by blinded, independent observers.

Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Neonatal Hypoxic-Ischemic Encephalopathy (HIE)
Device: Cool-Cap
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
235
September 2003
Not Provided

Inclusion Criteria:

Infants are assessed sequentially by criteria A, B and C listed below. Infant must meet all three criteria to be eligible for trial enrollment.

  • Criteria A: Infants >= 36 weeks gestation admitted to the NICU with ONE of the following:

    • Apgar score of <= 5 at 10 minutes after birth;
    • Continued need for resuscitation, including endotracheal or mask ventilation, at 10 minutes after birth;
    • Acidosis defined as either umbilical cord pH or any arterial pH within 60 minutes of birth < 7.00; or
    • Base Deficit <= -16 mmol/L in umbilical cord blood sample OR any blood sample within 60 minutes of birth (arterial or venous blood).
  • Criteria B: Moderate to severe encephalopathy consisting of altered state of consciousness (as shown by lethargy, stupor, or coma) AND at least one or more of the following:

    • Hypotonia;
    • Abnormal reflexes, including oculomotor or pupillary abnormalities;
    • An absent or weak suck;
    • Clinical seizures
  • Criteria C: At least 20 minutes duration of amplitude integrated EEG (aEEG/CFM) recording that shows abnormal background aEEG/CFM activity or seizures. The aEEG/CFM is to be performed from one hour of age. If subsequently an abnormal aEEG/CFM is recorded before 5.5 hours of age, the infant is then eligible for enrollment. The aEEG is not to be performed within 30 minutes of IV anticonvulsant therapy as this may cause suppression of EEG activity. In particular, high dose prophylactic anticonvulsant therapy (e.g., >20 mg/kg phenobarbitone) is not to be given prior to performing the aEEG/CFM.

Exclusion Criteria:

  • Infant expected to be > 5.5 hours of age at the time of randomization
  • Prophylactic administration of high dose anticonvulsants (e.g., >20 mg/kg phenobarbitone). After trial entry phenobarbitone or other anticonvulsant therapy is allowed to be given as clinically indicated to treat seizures.
  • Major congenital abnormalities, such as diaphragmatic hernia requiring ventilation, or congenital abnormalities suggestive of chromosomal anomaly or other syndromes that include brain dysgenesis
  • Imperforate anus
  • Evidence of head trauma or skull fracture causing major intracranial hemorrhage
  • Infant < 1,800 g birth weight
  • Head circumference < (mean - 2SD) for gestation if birth weight and length are > (mean - 2SD)
  • Infant "in extremis" (i.e. an infant for whom no other additional intensive management would be offered in the judgment of the attending neonatologist)
  • Unavailability of essential equipment (e.g., Cool-Cap, aEEG/CFM)
  • Planned concurrent participation in other experimental treatments
Both
up to 6 Hours
No
Contact information is only displayed when the study is recruiting subjects
United States,   Canada,   New Zealand,   United Kingdom
 
NCT00383305
IDE G990037, PMA P040025, HIE-0198
Not Provided
Not Provided
Olympic Medical
Not Provided
Principal Investigator: Peter D Gluckman, M.D. The Liggins Institute, University of Auckland; Auckland, New Zealand
Principal Investigator: John S. Wyatt, M.D. University College London; London, UK
Study Director: Alistair J Gunn, M.D., Ph.D. Department of Physiology, University of Auckland; Auckland, New Zealand
Olympic Medical
September 2006

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP