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Novel feeding system to promote the establishment of breastfeeding after preterm birth a randomised controlled trial.

Effect of a novel teat feeding system on breast feeding and length of hospital stay in preterm infants.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12614000875606
Enrollment
100
Registered
2014-08-14
Start date
2011-08-03
Completion date
2012-03-16
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

The use of the novel teat to feed expressed breastmilk when mother not available to breastfeed preterm baby resulted in a shorter length of stay in hospital (2.5 days corrected for gestational age at discharge (p=0.026) and weight (p=0.006). Infants in the novel teat group had less formula feeding a discharge (novel 35%, control 16%, p=0.036) but otherwise did not differ in respect to feeding.

Interventions

novel teat that releases milk only when the infant sucks with sufficient vacuum to release valve. The teat was offered only when mother was not available to breastfeed and when a bottle feed was scheduled, until discharge from hospital. Mother's expressed breastmilk was the feed of choice. Pastuerised donor human milk was available for those infants < 34 weeks gestation as an alternative and for those > 34 weeks, gestation, preterm formula was used when mother's expressed breastmilk was not avai

novel teat that releases milk only when the infant sucks with sufficient vacuum to release valve. The teat was offered only when mother was not available to breastfeed and when a bottle feed was scheduled, until discharge from hospital. Mother's expressed breastmilk was the feed of choice. Pastuerised donor human milk was available for those infants < 34 weeks gestation as an alternative and for those > 34 weeks, gestation, preterm formula was used when mother's expressed breastmilk was not available.

Sponsors

Women's and Newborns' health service, WA
Lead SponsorHospital

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
3 Days to 2 Months
Healthy volunteers
No

Inclusion criteria

preterm infants born at 25-34 weeks gestation at King Edward Hospital, Perth, and whose mothers intended to breastfeed

Exclusion criteria

congenital anomalies, grade 4 intraventricular haemorrhage or preiventricular malacia, oral anomaliess(tongue tie, cleft palate).

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026