Background: Despite therapeutic hypothermia (TH) and neonatal intensive care, 45–50% of children affected by moderate-to-severe neonatal hypoxic-ischemic encephalopathy (HIE) die or suffer from long-term neurodevelopmental impairment. Additional neuroprotective therapies are sought, besides TH, to further improve the outcome of affected infants. Allopurinol — a xanthine oxidase inhibitor — reduced the production of oxygen radicals and subsequent brain damage in pre-clinical and preliminary human studies of cerebral ischemia and reperfusion, if administered before or early after the insult. This ALBINO trial aims to evaluate the efficacy and safety of allopurinol administered immediately after birth to (near-)term infants with early signs of HIE. Methods/design: The ALBINO trial is an investigator-initiated, randomized, placebo-controlled, double-blinded, multi-national parallel group comparison for superiority investigating the effect of allopurinol in (near-)term infants with neonatal HIE. Primary endpoint is long-term outcome determined as survival with neurodevelopmental impairment versus death versus non-impaired survival at 2 years. Results: The primary analysis with three mutually exclusive responses (healthy, death, composite outcome for impairment) will be on the intention-to-treat (ITT) population by a generalized logits model according to Bishop, Fienberg, Holland (Bishop YF, Discrete Multivariate Analysis: Therory and Practice, 1975) and.”will be stratified for the two treatment groups. Discussion: The statistical analysis for the ALBINO study was defined in detail in the study protocol and implemented in this statistical analysis plan published prior to any data analysis. This is in accordance with the Declaration of Helsinki and the International Conference on Harmonization Good Clinical Practice guidelines.

Detailed statistical analysis plan for ALBINO: 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) / E. Corinna, R. Mario, B. Manon J N L, V.B. Frank, A. Karel, N. Gunnar, B. Dirk, K. Katrin, V. Maximo, V. Ana, F. Mari, M. Isabella, M. Marjo, V. Sampsa, M. Jan, M. Tuuli, V.D.V. Roselinda, F. Axel R, C. F Poets, H. Guimarães, T. Stiri, L. Cattarossi, C.K. W van Veldhuizen, C. A Maiwald, I. Bergmann, M. Weiss, A. Eichhorn, M. Raubuch, B. Schuler, B. Laméris, T. van Ramshorst, T. Kliniken, J. Brandner, M. Tackoen, R. Reibel, M. Ilmoja, P. Saik, R. Käär, P. Andresson, K.D.J. W Goethe, M. Rolf Schloesser, C. Gustav Carus, S. Winkler, T. Hoehn, N. Teig, M. Schroth, C. Fusch, U. H Thome, H. Ehrhardt, A. Virgilio Carnielli, M. Napolitano, F. Faldini, B. V Buzzi, M. Gianluca Lista, M. Barbarini, L. Pagani, E. Mastretta, G. Vento, M. Fumagalli, M. M van Weissenbruch, H.L. M van Straaten, K. V Annink, J. Dudink, J. B Derks, I. P de Boer, C. B Meijssen, T. R de Haan, L. G van Rooij, J. L van Hillegersberg, M. van Dongen, K. P Dijkman, M. A van Houten, S.R. D van der Schoor, M. Schneider, E. Nestaas, B. Nakstad, L. Karpinski, E. Gulczynska, C. Ferraz, A. Pereira, R. Barroso, M. da Graça, T. Tomé, F. Pinto, J. Martínez Rodilla, M. Luz Couce Pico, J. Antonio Hurtado Suazo, E. Valverde, J. Ramón Fernández Lorenzo, H. Boix, F. Jimenez Parrilla, D. Blanco, B. Loureiro, M. Teresa Moral-Pumarega, J. Maletzki, C. Knoepfli, C. Hagmann, M. Kleber, M. Stocker, T. Riedel. - In: TRIALS. - ISSN 1745-6215. - 25:1(2024 Jan 24), pp. 81.1-81.13. [10.1186/s13063-023-07828-6]

Detailed statistical analysis plan for ALBINO: 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)

M. Napolitano;M. Fumagalli;
2024

Abstract

Background: Despite therapeutic hypothermia (TH) and neonatal intensive care, 45–50% of children affected by moderate-to-severe neonatal hypoxic-ischemic encephalopathy (HIE) die or suffer from long-term neurodevelopmental impairment. Additional neuroprotective therapies are sought, besides TH, to further improve the outcome of affected infants. Allopurinol — a xanthine oxidase inhibitor — reduced the production of oxygen radicals and subsequent brain damage in pre-clinical and preliminary human studies of cerebral ischemia and reperfusion, if administered before or early after the insult. This ALBINO trial aims to evaluate the efficacy and safety of allopurinol administered immediately after birth to (near-)term infants with early signs of HIE. Methods/design: The ALBINO trial is an investigator-initiated, randomized, placebo-controlled, double-blinded, multi-national parallel group comparison for superiority investigating the effect of allopurinol in (near-)term infants with neonatal HIE. Primary endpoint is long-term outcome determined as survival with neurodevelopmental impairment versus death versus non-impaired survival at 2 years. Results: The primary analysis with three mutually exclusive responses (healthy, death, composite outcome for impairment) will be on the intention-to-treat (ITT) population by a generalized logits model according to Bishop, Fienberg, Holland (Bishop YF, Discrete Multivariate Analysis: Therory and Practice, 1975) and.”will be stratified for the two treatment groups. Discussion: The statistical analysis for the ALBINO study was defined in detail in the study protocol and implemented in this statistical analysis plan published prior to any data analysis. This is in accordance with the Declaration of Helsinki and the International Conference on Harmonization Good Clinical Practice guidelines.
Allopurinol; Brain injury; Cerebral palsy; Childbirth outcome; Hypothermia therapy; Hypoxic-ischemic encephalopathy; Neonatal oxygen deficiency; Perinatal asphyxia
Settore MEDS-20/A - Pediatria generale e specialistica
24-gen-2024
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1133322
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