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Safety and Efficacy of Topiramate in Neonates With Hypoxic Ischemic Encephalopathy Treated With Hypothermia (NeoNATI)

Primary Purpose

Hypoxic Ischemic Encephalopathy

Status
Completed
Phase
Phase 2
Locations
Italy
Study Type
Interventional
Intervention
Topiramate in newborns with hypoxic ischemic encephalopathy treated with therapeutic hypothermia
Sponsored by
Azienda Ospedaliero, Universitaria Meyer
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hypoxic Ischemic Encephalopathy focused on measuring asphyxia neonatorum, hypothermia, neuroprotection

Eligibility Criteria

36 Weeks - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Gestational age > 36 weeks and birth weigh > 1800 g with at least 1 of the following: a) Apgar score < 5 at 10 minutes; b) persisting need for resuscitation, including endotracheal intubation or mask ventilation 10 minutes after birth; c) acidosis (pH <7.0, base deficit >-16 mmol/L in umbilical cord blood or arterial, venous or capillary blood) within 60 minutes from birth;
  2. moderate to severe encephalopathy, consisting of altered state of consciousness (irritability, lethargy, stupor, or coma) and > 1 of the following sings: a) hypotonia, b) abnormal reflexes, including oculomotor or pupil abnormalities, c) absent or weak suck, d) clinical seizures.
  3. abnormal aEEG

Exclusion Criteria:

congenital abnormalities, congenital viral infections or evidence encephalopathy other than HIE.

-

Sites / Locations

  • Neonatal Intensive Care Unit - Azienda Ospedaliero-Universitaria Meyer
  • Neonatal Intensive Care Unit - Azienda Ospedaliero-Universitaria Pisana

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Topiramate

Control

Arm Description

Newborns with hypoxic ischemic encephalopathy treated with mild hypothermia and topiramate

Newborns with hypoxic ischemic encephalopathy treated with mild hypothermia

Outcomes

Primary Outcome Measures

The primary aim is to evaluate the neurological outcome at 6, 12, 18 months of life

Secondary Outcome Measures

The secondary aim is to evaluate the efficacy of treatment with topiramate for improving neuroradiological outcome at 3 and 12 months of life

Full Information

First Posted
November 10, 2010
Last Updated
December 12, 2013
Sponsor
Azienda Ospedaliero, Universitaria Meyer
Collaborators
Azienda Ospedaliero, Universitaria Pisana
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1. Study Identification

Unique Protocol Identification Number
NCT01241019
Brief Title
Safety and Efficacy of Topiramate in Neonates With Hypoxic Ischemic Encephalopathy Treated With Hypothermia
Acronym
NeoNATI
Official Title
Safety and Efficacy of Oral Topiramate in Neonates With Hypoxic Ischemic Encephalopathy Treated With Hypothermia: a Pilot Study of the Neonatal Neuroprotection of Asphyxiated Tuscan Infants (NeoNATI) Network
Study Type
Interventional

2. Study Status

Record Verification Date
December 2013
Overall Recruitment Status
Completed
Study Start Date
February 2010 (undefined)
Primary Completion Date
December 2013 (Actual)
Study Completion Date
December 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Azienda Ospedaliero, Universitaria Meyer
Collaborators
Azienda Ospedaliero, Universitaria Pisana

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine whether the administration of topiramate to newborns with hypoxic-ischemic encephalopathy potentiates the neuroprotective effect of treatment with hypothermia.
Detailed Description
Neonatal hypoxic-ischemic encephalopathy, due to perinatal asphyxia, is one of the leading causes of cerebral palsy, whose incidence, despite improvements in perinatal practice and neonatal care, has remained essentially unchanged over the recent past decades. It occurs approximately in 2-3 newborns every 1000 live births with a mortality rate of 10% for mild degrees and 60% for severe degrees. About 30% of survivors with mild hypoxic-ischemic encephalopathy and 100% with severe hypoxic-ischemic encephalopathy exhibit variable degrees of neurological disability. Several studies have demonstrated the therapeutic effects of whole-body or selective head cooling to treat neonates with hypoxic-ischemic encephalopathy. Mild hypothermia, (rectal or esophageal temperature 33-34°C), started within 6 h after birth and protracted for 48-72 h, can significantly improve primary outcome measures such as death or disability at 18 months or improve the neurological outcome in survivors. Consequently, mild hypothermia is at present recommended for the treatment of moderate degrees of encephalopathy. Topiramate an anticonvulsant agent widely used in adults and children, has been demonstrated to posses neuroprotective properties against hypoxic ischemic brain damage, both in vitro and in animal models and has been included in neuroprotective strategies for ischemic stroke and neonatal hypoxic-ischemic cerebral injury. Recently, topiramate treatment in asphyxiated newborns has been reported safe. Aim of the present study is to confirm the safety and to evaluate whether the association of topiramate enhances the neuroprotective properties of hypothermia for the treatment of neonatal hypoxic-ischemic encephalopathy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypoxic Ischemic Encephalopathy
Keywords
asphyxia neonatorum, hypothermia, neuroprotection

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
64 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Topiramate
Arm Type
Experimental
Arm Description
Newborns with hypoxic ischemic encephalopathy treated with mild hypothermia and topiramate
Arm Title
Control
Arm Type
No Intervention
Arm Description
Newborns with hypoxic ischemic encephalopathy treated with mild hypothermia
Intervention Type
Drug
Intervention Name(s)
Topiramate in newborns with hypoxic ischemic encephalopathy treated with therapeutic hypothermia
Intervention Description
TPM 10 mg/kg once a day will be administered with an orogastric tube as enteric-coated granules mixed with water on arrival in the NICU, when the cooling will be begun (T0), once a day for the first 3 days of life, for a total of 3 doses per patient.
Primary Outcome Measure Information:
Title
The primary aim is to evaluate the neurological outcome at 6, 12, 18 months of life
Time Frame
18 months of life
Secondary Outcome Measure Information:
Title
The secondary aim is to evaluate the efficacy of treatment with topiramate for improving neuroradiological outcome at 3 and 12 months of life
Time Frame
12 months of life

10. Eligibility

Sex
All
Minimum Age & Unit of Time
36 Weeks
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Gestational age > 36 weeks and birth weigh > 1800 g with at least 1 of the following: a) Apgar score < 5 at 10 minutes; b) persisting need for resuscitation, including endotracheal intubation or mask ventilation 10 minutes after birth; c) acidosis (pH <7.0, base deficit >-16 mmol/L in umbilical cord blood or arterial, venous or capillary blood) within 60 minutes from birth; moderate to severe encephalopathy, consisting of altered state of consciousness (irritability, lethargy, stupor, or coma) and > 1 of the following sings: a) hypotonia, b) abnormal reflexes, including oculomotor or pupil abnormalities, c) absent or weak suck, d) clinical seizures. abnormal aEEG Exclusion Criteria: congenital abnormalities, congenital viral infections or evidence encephalopathy other than HIE. -
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Luca Filippi, MD
Organizational Affiliation
Azienda Ospedaliero-Universitaria A. Meyer, Firenze, Italy
Official's Role
Principal Investigator
Facility Information:
Facility Name
Neonatal Intensive Care Unit - Azienda Ospedaliero-Universitaria Meyer
City
Florence
ZIP/Postal Code
I-50139
Country
Italy
Facility Name
Neonatal Intensive Care Unit - Azienda Ospedaliero-Universitaria Pisana
City
Pisa
ZIP/Postal Code
I-56100
Country
Italy

12. IPD Sharing Statement

Citations:
PubMed Identifier
19744111
Citation
Filippi L, la Marca G, Fiorini P, Poggi C, Cavallaro G, Malvagia S, Pellegrini-Giampietro DE, Guerrini R. Topiramate concentrations in neonates treated with prolonged whole body hypothermia for hypoxic ischemic encephalopathy. Epilepsia. 2009 Nov;50(11):2355-61. doi: 10.1111/j.1528-1167.2009.02302.x. Epub 2009 Sep 10.
Results Reference
background
PubMed Identifier
20553846
Citation
Filippi L, Poggi C, la Marca G, Furlanetto S, Fiorini P, Cavallaro G, Plantulli A, Donzelli G, Guerrini R. Oral topiramate in neonates with hypoxic ischemic encephalopathy treated with hypothermia: a safety study. J Pediatr. 2010 Sep;157(3):361-6. doi: 10.1016/j.jpeds.2010.04.019. Epub 2010 May 31.
Results Reference
background
PubMed Identifier
24524452
Citation
Shankaran S. Outcomes of hypoxic-ischemic encephalopathy in neonates treated with hypothermia. Clin Perinatol. 2014 Mar;41(1):149-59. doi: 10.1016/j.clp.2013.10.008.
Results Reference
derived
PubMed Identifier
22950861
Citation
Filippi L, Fiorini P, Daniotti M, Catarzi S, Savelli S, Fonda C, Bartalena L, Boldrini A, Giampietri M, Scaramuzzo R, Papoff P, Del Balzo F, Spalice A, la Marca G, Malvagia S, Della Bona ML, Donzelli G, Tinelli F, Cioni G, Pisano T, Falchi M, Guerrini R. Safety and efficacy of topiramate in neonates with hypoxic ischemic encephalopathy treated with hypothermia (NeoNATI). BMC Pediatr. 2012 Sep 5;12:144. doi: 10.1186/1471-2431-12-144.
Results Reference
derived
Links:
URL
http://druginfo.nlm.nih.gov/
Description
Drug information

Learn more about this trial

Safety and Efficacy of Topiramate in Neonates With Hypoxic Ischemic Encephalopathy Treated With Hypothermia

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