Effect of supplementary pasteurised donor human milk compared with standard formula on time to full enteral feeds, feed tolerance, growth, breastfeeding and length of hospital stay in moderate and late preterm babies – a pilot randomised controlled trial

South Australia Health and Medical Research Institute0 个研究点目标入组 201 人开始时间: 2021年5月6日最近更新: 2024年3月25日

适应症

试验速览

Findings are currently being written up for publication in peer reviewed journals and other formats.

•Eligible infants must meet all of the following criteria:
•1. 32+0 and 36+6 completed weeks’ gestation at birth;
•2. Birth weight 1500g or more;
•3, Admitted to the neonatal unit;
•4. Clinically stable;
•5. Ready to commence enteral feeds or commenced enteral feeds with human milk but insufficient maternal breast milk is available;
•6. Aged less than or equal to 4 days old;
•7. Has a parent or guardian capable of giving informed consent.

•An infant who meets any of the following criteria will be excluded from participation:
•1. Metabolic disorder that precludes breastfeeding;
•2. Major congenital malformation either likely to interfere with the ability to ingest milk or requiring surgery in the first 6 months of life;
•3. Given infant formula prior to randomisation.

发起方

South Australia Health and Medical Research Institute