Yin Li-Ping, Qian Li-Juan, Zhu Huan, Chen Yan, Li Han, Han Ji-Nan, Qiao Li-Xing
Department of Paediatrics, Zhongda Hospital Southeast University, 87 Dingjiaqiao, Nanjing, 210009, China.
Trials. 2015 Nov 4;16:498. doi: 10.1186/s13063-015-1030-5.
The average incidence of preterm birth in the world is up to 11.1 %, and deaths of preterm children account for more than 50 % of neonatal deaths. Gastrointestinal function of preterm children with a gestational age less than 34 weeks is immaturely developed. For preterm children who can only be fed with formula due to their mothers' sickness, choosing a suitable formula can not only meet the high nutritional needs of preterm children, but also solve their low gastrointestinal tolerability, and is thus very important.
METHODS/DESIGN: The study is a prospective, randomized, single-blind and controlled clinical trial. Preterm children with a gestational age less than 34 weeks meeting the inclusion criteria who cannot be breastfed will be included. To demonstrate the application effect of extensively hydrolyzed milk protein formula on the target population, preterm children will be randomized into two groups, 185 subjects in each group. The observation group will be fed with extensively hydrolyzed milk protein (100 % whey protein) formula, while the control group will be fed with preterm children's formula until the children are discharged from the neonatal intensive care unit (NICU). All the formula involved in this study will be from Dumex. After discharge, both groups will be uniformly fed with formula for 0 to 6-month-old infants. For statistical analysis, a chi-square test and Student's t test will be applied using SAS 9.4.
This will be the first randomized controlled clinical study with long-term observation of the growth and development of preterm children during the NICU stay and at 3-month follow-up after discharge from the NICU. Results from this study will be used to determine whether the extensively hydrolyzed formula is more suitable for the low gastrointestinal tolerability of preterm children, and also whether feeding preterm children who are fed with such formula during the NICU stay with ordinary infant formula after discharge from the NICU would affect the normal growth and development of preterm children in the early stage of their lives.
This study was registered with the Chinese Clinical Trial Registry ( http://www.chictr.org.cn/ ) with number ChiCTR-IOR-14005696 , on December 22, 2014.
全球早产平均发生率高达11.1%,早产儿童死亡占新生儿死亡的50%以上。孕周小于34周的早产儿童胃肠功能发育不成熟。对于因母亲患病只能喂配方奶的早产儿童,选择合适的配方奶不仅能满足其高营养需求,还能解决其胃肠耐受性低的问题,因此非常重要。
方法/设计:本研究是一项前瞻性、随机、单盲对照临床试验。纳入孕周小于34周、符合纳入标准且无法母乳喂养的早产儿童。为证明深度水解乳蛋白配方奶对目标人群的应用效果,将早产儿童随机分为两组,每组185例。观察组喂深度水解乳蛋白(100%乳清蛋白)配方奶,对照组喂早产儿童配方奶,直至儿童从新生儿重症监护病房(NICU)出院。本研究涉及的所有配方奶均来自多美滋。出院后,两组均统一喂0至6个月婴儿配方奶。采用SAS 9.4进行统计分析,应用卡方检验和t检验。
这将是第一项对早产儿童在NICU住院期间及NICU出院后3个月随访时的生长发育进行长期观察的随机对照临床研究。本研究结果将用于确定深度水解配方奶是否更适合胃肠耐受性低的早产儿童,以及在NICU住院期间喂这种配方奶的早产儿童出院后喂普通婴儿配方奶是否会影响其生命早期的正常生长发育。
本研究于2014年12月22日在中国临床试验注册中心(http://www.chictr.org.cn/)注册,注册号为ChiCTR-IOR-14005696。