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Study of Cerebrolysin for Treatment of Infants With History of Neonatal Hypoxic Ischemic Encephalopathy (CerebroHIE)

S

Sahar M.A. Hassanein, MD

Status and phase

Completed
Phase 2

Conditions

Hypoxic-Ischemic Encephalopathy

Treatments

Drug: Cerebrolysin®

Study type

Interventional

Funder types

Other

Identifiers

NCT01059461
IRB 00006379

Details and patient eligibility

About

The purpose of this study is to determine whether nerve growth factor (cerebrolysin®) therapy will improve the psychomotor outcome in infants with moderate and severe hypoxic ischemic encephalopathy after hospital discharge.

Full description

Infants with perinatal history of moderate to severe Hypoxic ischemic encephalopathy HIE will receive 10 injections of cerebrolysin IM. Assessment of neurodevelopment will be done before , 3 and 6 months after therapy

Enrollment

40 estimated patients

Sex

All

Ages

3 to 6 months old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

*Inclusion Criteria: Infant aged 3-6 months with perinatal history of moderate or severe HIE collected from his NICU's file. Criteria of neonatal asphyxia and encephalopathy according to the American College of Obstetricians and Gynecologist and American Academy of Pediatrics, metabolic acidosis with a cord pH of 7.0 or less or a base deficit of at least 12 mmol/L, early onset of encephalopathy, and multisystem organ dysfunction with exclusion of other possible causes for findings.

Criteria of neonatal asphyxia:

  • Full term neonate more than 36 weeks of gestation
  • pH of 7.0 or less or a base deficit of 16 mmol per liter or more in a sample of umbilical-cord blood or any blood during the first hour after birth.
  • If, during this interval, a pH is between 7.01 and 7.15, a base deficit is between 10 and 15.9 mmol per liter, or a blood gas is not available, additional criteria are required. These includes an acute perinatal event (e.g., late or variable decelerations, cord prolapse, cord rupture, uterine rupture, maternal trauma, hemorrhage, or cardiorespiratory arrest) and either a 10-minute Apgar score of 5 or less or assisted ventilation initiates at birth and continues for at least 10 minutes.

Criteria of neonatal encephalopathy according to Sarnat and Sarnat. Presence of one or more signs in at least three of the following six categories:

  • level of consciousness.

  • spontaneous activity.

  • posture.

  • tone.

  • primitive reflexes (suck or Moro.

  • autonomic nervous system (pupils, heart rate, or respiration). The number of moderate or severe signs determined the extent of encephalopathy; if signs were equally distributed, the designation was based on the level of consciousness.

    *Exclusion Criteria:

  • Severe intrauterine growth retardation.

  • Congenital malformations.

  • Suspected inborn error of metabolism.

  • Suspected inherited neurologic disease.

  • Intracranial hemorrhage

  • Meningitis

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

40 participants in 1 patient group

Cerebrolysin®, neuroregeneration
Experimental group
Description:
Injection of cerebrolysin® 0.1ml/kg IM twice weekly for 10 injections after discharge from NICU (postneonatal)
Treatment:
Drug: Cerebrolysin®

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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