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

Phase 2 Nerve Growth Factor (Cerebrolysin®) for Treatment of Neonatal Hypoxic Ischemic Encephalopathy

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01059461
Acronym
CerebroHIE
Enrollment
40
Registered
2010-02-01
Start date
2011-03-31
Completion date
2013-09-30
Last updated
2013-09-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypoxic-Ischemic Encephalopathy

Keywords

Hypoxic Ischemic Encephalopathy (HIE), Perinatal Asphyxia, Nerve growth factor, Cerebrolysin, Cerebral palsy

Brief summary

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.

Detailed 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

Interventions

DRUGCerebrolysin®

injection of cerebrolysin® 0.1ml/kg IM twice weekly for 10 injections after discharge from NICU (postneonatal)

Sponsors

Sahar M.A. Hassanein, MD
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
3 Months to 6 Months
Healthy volunteers
No

Inclusion 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

Design outcomes

Primary

MeasureTime frameDescription
Side effects during cerebrolysin therapy (one course).3 monthsweekly physical , neurological examination and parents' reported fever or convulsion during cerebrolysin injection course (10 injections).

Secondary

MeasureTime frame
Neurodevelopmental follow up after 6 and 9 months of cerebrolysin injection.9 months

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026