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Detailed statistical analysis plan for the SafeBoosC III trial: a multinational randomised clinical trial assessing treatment guided by cerebral oxygenation monitoring versus treatment as usual in extremely preterm infants.
Hansen, Mathias Lühr; Pellicer, Adelina; Gluud, Christian; Dempsey, Eugene; Mintzer, Jonathan; Hyttel-Sorensen, Simon; Heuchan, Anne Marie; Hagmann, Cornelia; Dimitriou, Gabriel; Pichler, Gerhard; Naulaers, Gunnar; Cheng, Guoqiang; Vilan, Ana; Tkaczyk, Jakub; Kreutzer, Karen B; Fumagalli, Monica; Claris, Olivier; Fredly, Siv; Szczapa, Tomasz; Lange, Theis; Jakobsen, Janus Christian; Greisen, Gorm.
Afiliação
  • Hansen ML; Department of Neonatology, Rigshospitalet, Copenhagen University Hospital, Blegdamsvej 9, 2100, Copenhagen, Denmark. mathias.safeboosc@gmail.com.
  • Pellicer A; Department of Neonatology, La Paz University Hospital, Paseo De La Castellana 261, 28046, Madrid, Spain.
  • Gluud C; Copenhagen Trial Unit, Centre for Clinical Intervention Research, Rigshospitalet, Copenhagen University Hospital, Blegdamsvej 9, 2100, Copenhagen, Denmark.
  • Dempsey E; Infant Centre and Department of Paediatrics and Child Health, University College Cork, College Road, Cork, Ireland.
  • Mintzer J; Division of Neonatal-Perinatal Medicine, Mountainside Medical Center, Montclair, NJ, USA.
  • Hyttel-Sorensen S; Department of Neonatology, Rigshospitalet, Copenhagen University Hospital, Blegdamsvej 9, 2100, Copenhagen, Denmark.
  • Heuchan AM; Department of Neonatology, Royal Hospital for Children, 1345 Govan Rd, Glasgow, G51 4TF, UK.
  • Hagmann C; Department of Neonatology, Children's University Hospital of Zürich, Steinweisstrasse 75, 8037, Zurich, Switzerland.
  • Dimitriou G; NICU, Department of Pediatrics, University General Hospital of Patras, 265 04, Patras, Greece.
  • Pichler G; Department of Pediatrics, Medical University of Graz, Auenbruggerplatz 30, Graz, Austria.
  • Naulaers G; Department of Neonatology, University Hospital Leuven, Herestraat 49, Leuven, Belgium.
  • Cheng G; Department of Neonatology, Children's Hospital of Fudan University, 399 Wanyuan Rd, Minhang Qu, Shanghai Shi, China.
  • Vilan A; Department of Neonatology, Centrohospitalar Universitário de São João, Alameda Prof. Hernâni Monteiro, 4200-319, Porto, Portugal.
  • Tkaczyk J; Department of Neonatology, University Hospital Motol, V Uvalu 84, 150 06, Prague 5, Czech Republic.
  • Kreutzer KB; Department of Neonatology, University Children's Hospital Tuebingen, Hoppe-Seyler-Straße 1, 72076, Tuebingen, Germany.
  • Fumagalli M; Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico Milan, Via della Commenda 12, 20122, Milan, Italy.
  • Claris O; Department of Clinical Sciences and Community Health, University of Milan, Milan, Italy.
  • Fredly S; Department of Neonatology, Hospices Civil De Lyon, 3 Quai des Célestins, 69002, Lyon, France.
  • Szczapa T; Department of Neonatology, Oslo University Hospital, Kirkeveien, 166 0450, Oslo, Norway.
  • Lange T; Department of Neonatology, Poznan University of Medical Sciences, Polna 33, 60-535, Poznan, Poland.
  • Jakobsen JC; Section of Biostatistics, Department of Publich Health, Copenhagen University, Øster Farimagsgade 5, Copenhagen K, Denmark.
  • Greisen G; Center for Statistical Science, Peking University, Beijing, China.
Trials ; 20(1): 746, 2019 Dec 19.
Article em En | MEDLINE | ID: mdl-31856902
ABSTRACT

BACKGROUND:

Infants born extremely preterm are at high risk of dying or suffering from severe brain injuries. Treatment guided by monitoring of cerebral oxygenation may reduce the risk of death and neurologic complications. The SafeBoosC III trial evaluates the effects of treatment guided by cerebral oxygenation monitoring versus treatment as usual. This article describes the detailed statistical analysis plan for the main publication, with the aim to prevent outcome reporting bias and data-driven analyses. METHODS/

DESIGN:

The SafeBoosC III trial is an investigator-initiated, randomised, multinational, pragmatic phase III trial with a parallel group structure, designed to investigate the benefits and harms of treatment based on cerebral near-infrared spectroscopy monitoring compared with treatment as usual. Randomisation will be 11 stratified for neonatal intensive care unit and gestational age (lower gestational age (< 26 weeks) compared to higher gestational age (≥ 26 weeks)). The primary outcome is a composite of death or severe brain injury at 36 weeks postmenstrual age. Primary analysis will be made on the intention-to-treat population for all outcomes, using mixed-model logistic regression adjusting for stratification variables. In the primary analysis, the twin intra-class correlation coefficient will not be considered. However, we will perform sensitivity analyses to address this. Our simulation study suggests that the inclusion of multiple births is unlikely to significantly affect our assessment of intervention effects, and therefore we have chosen the analysis where the twin intra-class correlation coefficient will not be considered as the primary analysis.

DISCUSSION:

In line with the Declaration of Helsinki and the International Conference on Harmonization Good Clinical Practice guidelines, we have developed and published this statistical analysis plan for the SafeBoosC III trial, prior to any data analysis. TRIAL REGISTRATION ClinicalTrials.org, NCT03770741. Registered on 10 December 2018.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Oxigênio / Encéfalo / Hipóxia Encefálica / Tratamento de Emergência / Lactente Extremamente Prematuro / Monitorização Fisiológica Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Oxigênio / Encéfalo / Hipóxia Encefálica / Tratamento de Emergência / Lactente Extremamente Prematuro / Monitorização Fisiológica Idioma: En Ano de publicação: 2019 Tipo de documento: Article