Effect of Allopurinol for Hypoxic-ischemic Brain Injury on Neurocognitive Outcome

Infant, Newborn, Diseases Clinical Trial

— ALBINO  

Official title:

Effect of ALlopurinol in Addition to Hypothermia for Hypoxic-ischemic Brain Injury on Neurocognitive Outcome - a Blinded Randomized Placebo-controlled Parallel Group Multicenter Trial for Superiority (Phase III)

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03162653
• Other study ID #: ALBINO
• Secondary ID: 2016-000222-19
• Status: Recruiting
• Phase: Phase 3
• Start date: March 25, 2018
• Est. completion date: January 31, 2026

Study information

• Verified date: July 2023
• Source: University Hospital Tuebingen
• Contact: Oldershausen Gabriele
• Phone: +49 7071 29-86176
• Email: Albino[@]med.uni-tuebingen.de
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Neonatal hypoxic-ischemic encephalopathy (HIE) is a major cause of death or long-term disability in infants born at term in the western world, affecting about 1-4 per 1.000 life births and consequently about 5-20.000 infants per year in Europe. Hypothermic treatment became the only established therapy to improve outcome after perinatal hypoxic-ischemic insults. Despite hypothermia and neonatal intensive care, 45-50% of affected children die or suffer from long-term neurodevelopmental impairment. Additional neuroprotective interventions, beside hypothermia, are warranted to further improve their outcome. Allopurinol is a xanthine oxidase inhibitor and reduces the production of oxygen radicals and brain damage in experimental, animal, and early human studies of ischemia and reperfusion. This project aims to evaluate the efficacy and safety of allopurinol administered immediately after birth to near-term infants with HIE in addition to hypothermic treatment.

Description:

During labour and childbirth various events (such as placental abruption, uterine rupture, umbilical cord complications etc.) may result in impaired oxygenation and/or perfusion of the newborn brain which may result in brain injury termed "hypoxic-ischemic encephalopathy" (HIE). HIE is associated with development of long-term motor, cognitive, and neurosensory and memory disability and is one of the fundamental problems in perinatal medicine affecting about 5,000-20,000 infants/year in Europe (or 1-4/1000 live births in western societies) and approximately 1 million infants/year worldwide. In term infants with perinatal asphyxia and postnatal HIE, brain injury predominantly originates in the immediate perinatal period (in contrast to a more distant prenatally acquired brain injury) as indicated by the lack of already established brain injury on early postnatal MRI. Consequently, brain injury in this population may potentially be ameliorated by postnatal pharmacological interventions. The most common motor disability resulting from HIE is "cerebral palsy", the other major adverse outcome is cognitive disability, which prevents affected patients to lead their lives independently (without assistance and/or financial support). The single major cause of HIE is a perinatal hypoxic/ischemic event (perinatal asphyxia). This hypoxic insult can cause immediate (necrosis) and delayed death (apoptosis) of (especially neuronal) cells, the latter responsible for a substantial amount of HIE-associated permanent brain damage. Whereas no intervention is known to prevent necrosis, the delayed cell death by apoptosis can be reduced by therapeutic interventions: Apoptosis is in part caused by secondary energy failure which can be reduced by hypothermic treatment. Apoptosis is also caused by xanthine oxidase-mediated production of cytotoxic oxygen radicals during reperfusion, and there is evidence that allopurinol, a xanthine-oxidase inhibitor, reduces delayed cell death in animal models of perinatal asphyxia and ischemia/reperfusion. Allopurinol prevents adenosine degradation, oxygen radical formation, preserves NMDA receptor integrity, and consequently may reduce brain injury in HIE by several mechanisms of action which are independent from the proven beneficial effect of hypothermic treatment on cellular energy metabolism. An additional beneficial (or even synergistic?) effect of allopurinol in addition to hypothermia can therefore be expected. As no safety concerns were known at the start of this study regarding administration of even high doses of Allopurinol to neonates a phase III study was planned instead of a pilot study or an adaptive design. Close follow-up of MR-imaging along with reporting of all safety relevant data to a Data Monitoring Committee (which includes experts for brain imaging not otherwise involved in the study) ensures patients' safety. Primary objective of this study is to evaluate whether newborns with asphyxia and early clinical signs of hypoxic ischemic encephalopathy will benefit from early administered Allopurinol compared to placebo, both in addition to standard of care, regarding long-term follow-up such as severe neurodevelopmental impairment or death at two years.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 760
• Est. completion date: January 31, 2026
• Est. primary completion date: January 31, 2026
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A to 45 Minutes

Eligibility

Inclusion criteria Term and near-term infants with a history of disturbed labour who meet at least one criterion of perinatal acidosis (or ongoing resuscitation) and at least two early clinical signs of potentially evolving encephalopathy as defined herein: Severe perinatal metabolic acidosis or ongoing cardiopulmonary resuscitation at 5 min after birth: At least 1 out of the following 5 criteria must be met

• Umbilical (or arterial or reliable venous) blood gas within 30 min after birth with pH<7.0
• Umbilical (or arterial or reliable venous) blood gas within 30 min after birth with base deficit =16 mmol/l
• Need for ongoing cardiac massage at/beyond 5 min postnatally
• Need for adrenalin administration during resuscitation
• APGAR score =5 at 10min AND Early clinical signs of potentially evolving encephalopathy:

At least 2 out of the following 4 criteria must be met:

• Altered state of consciousness (reduced or absent response to stimulation or hyperexcitability)
• Severe muscular hypotonia or hypertonia,
• Absent or insufficient spontaneous respiration (e.g., gasping only) with need for respiratory support at 10 min postnatally
• Abnormal primitive reflexes (absent suck or gag or corneal or Moro reflex) or abnormal movements (e.g., potential clinical correlates of seizure activity) Exclusion criteria
• gestational age below 36 weeks
• birth weight below 2500 g
• postnatal age >30min at the end of screening phase
• severe congenital malformation or syndrome requiring neonatal surgery or affecting long-term outcome
• patient considered "moribund" / "non-viable" (e.g., lack of spontaneous cardiac activity and ongoing chest compression at 30min)
• decision for "comfort care only" before study drug administration
• parents declined study participation as response to measures of community engagement
• both parents are insufficiently fluent in the study site's national language(s) or English or do not seem to have the intellectual capacity to understand the study procedures and to give consent as judged by the personnel who had been in contact with the mother/father before delivery.
• both parents/guardians less than 18 years of age, in case of single parent/guardian this one less than 18 years of age

Related Conditions & MeSH terms

• Brain Diseases
• Brain Injuries
• Encephalopathy, Hypoxic-Ischemic
• Hypoxia
• Hypoxia, Brain
• Hypoxia-Ischemia, Brain
• Infant, Newborn, Diseases
• Ischemia

Intervention

Drug:
• Allopurinol
Allopurinol, powder for injection (PFI), administered in two doses. First dose (20 mg/kg in 2ml/kg sterile water for injection) given as soon as intravenous access is established and no later than 30min postnatally and second dose (10mg/kg in 1ml/kg sterile water for injection) 12 hours thereafter. The second dose will only be administered to in infants on therapeutic hypothermia. Infants who recover quickly and do not qualify for and hence do not undergo hypothermia will not receive a second dose. Administration will be by continuous infusion using a syringe pump over 10min through secure venous access.
• Mannitol
Placebo (Mannitol, PFI, 20mg/kg in the same volume and at the same time intervals as the intervention group - (2nd dose 10mg/kg only if infant undergoes therapeutic hypothermia)).

Locations

Country	Name	City	State
Austria	Medizinische Universitaet Wien	Wien
Belgium	Katholieke Universiteit Leuven	Leuven
Estonia	Tartu Ulikool	Tartu
Finland	Helsingin Ja Uudenmaan Sairaanhoitopiirin Kuntayhtymä	Helsinki
Germany	University Hospital Tübingen	Tübingen
Italy	Universita Degli Studi Di Udine	Udine
Netherlands	Universitair Medisch Centrum Utrecht	Utrecht
Norway	Oslo Universitetssykehus Hf	Oslo
Poland	Uniwersytet Medyczny Im Karola Marcinkowskiego W Poznaniu	Poznan
Portugal	Universidade Do Porto	Porto
Spain	Para La Investigacion Del Hospital UniversitarioLa Fe De La Comunidad Valenciana	Valencia
Switzerland	Universitaet Zuerich	Zuerich

Sponsors (15)

Lead Sponsor

Collaborator

University Hospital Tuebingen

ACE Pharmaceuticals BV, Fundación para la Investigación del Hospital Clínico de Valencia, Helsingin Ja Uudenmaan Sairaanhoitopiirin, KU Leuven, Oslo University Hospital, Poznan University of Medical Sciences, Tartu University Hospital, Technische Universität Dresden, UMC Utrecht, Universidade do Porto, Università degli Studi di Udine, University of Helsinki, University of Vienna, University of Zurich

Countries where clinical trial is conducted

Austria,  Belgium,  Estonia,  Finland,  Germany,  Italy,  Netherlands,  Norway,  Poland,  Portugal,  Spain,  Switzerland, 

References & Publications (3)

Annink KV, Franz AR, Derks JB, Rudiger M, Bel FV, Benders MJNL. Allopurinol: Old Drug, New Indication in Neonates? Curr Pharm Des. 2017;23(38):5935-5942. doi: 10.2174/1381612823666170918123307. — View Citation

Deferm N, Annink KV, Faelens R, Schroth M, Maiwald CA, Bakkali LE, van Bel F, Benders MJNL, van Weissenbruch MM, Hagen A, Smits A, Annaert P, Franz AR, Allegaert K; ALBINO Study Group. Glomerular Filtration Rate in Asphyxiated Neonates Under Therapeutic Whole-Body Hypothermia, Quantified by Mannitol Clearance. Clin Pharmacokinet. 2021 Jul;60(7):897-906. doi: 10.1007/s40262-021-00991-6. Epub 2021 Feb 21. — View Citation

Maiwald CA, Annink KV, Rudiger M, Benders MJNL, van Bel F, Allegaert K, Naulaers G, Bassler D, Klebermass-Schrehof K, Vento M, Guimaraes H, Stiris T, Cattarossi L, Metsaranta M, Vanhatalo S, Mazela J, Metsvaht T, Jacobs Y, Franz AR; ALBINO Study Group. Effect of allopurinol in addition to hypothermia treatment in neonates for hypoxic-ischemic brain injury on neurocognitive outcome (ALBINO): study protocol of a blinded randomized placebo-controlled parallel group multicenter trial for superiority (phase III). BMC Pediatr. 2019 Jun 27;19(1):210. doi: 10.1186/s12887-019-1566-8. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	death versus severe neurodevelopmental impairment versus survival without severe neurodevelopmental impairment	Where severe neurodevelopmental impairment is defined as any of the following: cognitive or language delay defined as a cognitive-composite-score or a language-composite-score on the Bayley Scales of Infant and Toddler Development (3rd edition) < 85 and/or cerebral palsy (CP) according to SCPE criteria [SCPE Dev Med Child Neurol 2000]. In case of missing Bayley III test results, Bayley II or other developmental test results or PARCA-R parent questionnaire results may substitute for the Bayley III test result in a predefined hierarchical order.; Primary endpoint with three mutually exclusive responses (healthy, death, composite outcome for impairment) will be analyzed in the two treatment groups by a generalized logits model according to Bishop, Fienberg, Holland 1975 with SAS 9.4 procedure proc catmod.	at the age of 24 months
Secondary	Death or neurodevelopmental impairment (NDI)	The primary endpoint will be reconstituted as dichotomised composite secondary endpoint (survival without NDI versus Death or language-composite-score < 85 or cognitive-composite score <85 or cerebral palsy present). In case of missing Bayley III test results, Bayley II or other developmental test results or PARCA-R parent questionnaire results may substitute for the Bayley III test result in a predefined hierarchical order.; This will be analyzed by Cochrane-Mantel-Haenszel- X²-Test.	at 24months
Secondary	Incidence of Death	Incidence of death will be analyzed by Cochrane-Mantel-Haenszel- X²-Test.	at 24 months
Secondary	Incidence of CP	Incidence of CP according to SCPE criteria [SCPE Dev Med Child Neurol 2000] will be analyzed by Cochrane-Mantel-Haenszel- X²-Test.	at 24 months
Secondary	GMFCS-score	GMFCS-Score for quantification of the effects of cerebral palsy and other motor impairments (adapted from Palisano et al. [Palisano Med Child Neurol 1997]) using the ALBINO-GMFCS-score sheet will be analysed. GMFCS-score consists of six categories. Analysis will be done by using Wilcoxon-Mann-Whitney test.	at 24 months
Secondary	Motor-Composite-Score (Bayley III)	The numerical data of the motor-composite-score will be analysed using Wilcoxon-Mann-Whitney test. The use of this test accounts for the fact that data will be cut due to lack of sensitivity below 50 points.	at 24 months
Secondary	Motor-Composite-Score dichotomised (Bayley III)	The motor-composite-score will be dichotomised at the cut-off <85 versus =85 and analysed by Cochrane-Mantel-Haenszel- X²-Test.	at 24 months
Secondary	Cognitive-Composite-Score (cognitive subscale, Bayley III)	The numerical data of the cognitive-composite-score will be analysed using Wilcoxon-Mann-Whitney test. The use of this test accounts for the fact that data will be cut due to lack of sensitivity below 50 points.	at 24 months
Secondary	Cognitive-Composite-Score dichotomised (cognitive subscale, Bayley III)	The cognitive-composite-score will be dichotomised at the cut-off <85 versus =85 and analysed by Cochrane-Mantel-Haenszel- X²-Test.	at 24 months
Secondary	Language-Composite-Score (language subscale, Bayley III)	The raw numerical data of the language-composite-score will be analysed using Wilcoxon Mann-Whitney test. The use of this test accounts for the fact that data will be cut due to lack of sensitivity below 50 points.	at 24 months
Secondary	Language-Composite-Score dichotomised (language subscale, Bayley III)	The language-composite-score will be dichotomised at the cut-off <85 versus =85 and analysed by Cochrane-Mantel-Haenszel- X²-Test	at 24 months

External Links

•   official study homepage