Avoiding routine gastric residual volume measurement in neonatal critical care (the neoGASTRIC trial): study protocol for a multi-centre, unblinded, randomised, controlled trial.
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Nuthall Elizabeth, Rodriquez Amy, Andrzejewksa Iza, Aslam Zainab, Battersby Cheryl, Beesley Catherine, Cole Christina, Campbell Helen, Dalziel Kim, Dorling Jon, Downs Alan, Davis Peter G, Daskalopoulou Zoe, Forster Amanda, Graham-Travis Michaela, Hall Nigel J, Hubbard Marie, Hurd Madeleine, Hardy Pollyanna, Hunt Rod, Kennedy Ann, King Andrew, Linsell Louise, Manley Brett J, Murray David, Mitchell Tracy K, O'Connor Heather, Ojha Shalini, Roehr Charles C, Rivero-Arias Oliver, Stanbury Kayleigh, Taylor Jacqueline, Tume Lyvonne, Welsh Richard, Wiles Joy, Woolfall Kerry, Young Lauren, Roberts Calum, Gale Chris, neoGASTRIC collaborative group
Аннотация
METHODS: The aim of the neoGASTRIC trial is to test whether avoiding routine measurement of gastric residual volumes in preterm infants reduces the time taken for an infant to reach full enteral feeds without increasing necrotising enterocolitis. neoGASTRIC is an individually randomised controlled trial in neonatal units in the UK and Australia. A target of 7040 infants born before 34 weeks' gestation will be randomly allocated, prior to receiving 24 h of enteral feeds > 15 ml/kg/day, on a 1:1 basis to have no routine gastric residual volumes measured, or to have gastric residual volumes measured routinely. Opt-out consent will be used with parent and staff views explored as part of an embedded process evaluation. The primary superiority outcome is time to reach full milk feeds ≥ 145 ml/kg/day for three consecutive days. Bell's stage 2 or 3 necrotising enterocolitis following blinded adjudication will be the key secondary, non-inferiority safety outcome. Other neonatal core outcomes and health care resource use and costs prior to discharge will be evaluated.
DISCUSSION: neoGASTRIC will address a research priority that affects more than 20,000 preterm infants in the United Kingdom and Australia annually. Even modest improvements in clinical outcomes and resource use could result in large clinical benefits and savings at a population level.
TRIAL REGISTRATION: ISRCTN 16710849 . Prospectively registered on 8 February 2023.