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Implementation of a guideline in babies on postnatal wards

Local clinical leaders to implement a national guideline in babies on postnatal wards: a cluster-randomised, blinded, controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN61154098
Enrollment
1250
Registered
2015-05-20
Start date
2015-06-01
Completion date
Unknown
Last updated
2023-10-09

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

Conditions

Neonatal hypoglycaemia Pregnancy and Childbirth Other neonatal hypoglycaemia

Interventions

Current interventions as of 01/02/2022: Participating hospitals will be randomised: 1. Medical leader to implement a guideline on oral dextrose gel to treat neonatal hy

Sponsors

University of Auckland
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Doctors and midwives attached to New Zealand maternity hospitals with >50 births/year where babies are at risk of neonatal hypoglycaemia (infant of a diabetic, late preterm, small or large for gestational age) are delivered, including hospitals where oral dextrose gel is currently in use.

Exclusion criteria

Exclusion criteria: Hospitals in NZ without a doctor (paediatrician or general practitioner) available to provide medical treatment, or no midwifery care for newborn babies.

Design outcomes

Primary

MeasureTime frame
The change in the proportion of eligible hypoglycaemic babies treated with dextrose gel before implementation of the dextrose gel guideline to three months after implementation.

Secondary

MeasureTime frame
Current secondary outcome measures as of 01/02/2022: 1. Proportion of eligible babies admitted to NICU for at least 4 hours 2. Proportion of eligible babies given formula as a treatment for hypoglycaemia during hospital admission 3. Amount of dextrose gel used in the hospital 4. Prolonged uptake of dextrose gel (change in proportion of eligible babies treated with dextrose gel before implementation of the guideline to 6 months after implementation) 5. Sustained use of dextrose gel (change in proportion of eligible babies treated with dextrose gel from 3 months after implementation to 6 months after implementation) 6. Successful treatment with oral dextrose gel on the blood test taken immediately following dextrose gel treatment 7. Adherence to the 'oral dextrose gel to treat neonatal hypoglycaemia guideline' 8. Breastfeeding at discharge Previous secondary outcome measures: 1. Proportion of eligible babies admitted to NICU for at least 4 hours 2. Proportion of eligible babies given formula as a treatment for hypoglycaemia during hospital admission 3. Amount of dextrose gel used in the hospital 4. Initial uptake of dextrose gel (change in proportion of eligible babies treated with dextrose gel before implementation of the guideline to 1 month after implementation) 5. Sustained use of dextrose gel (change in proportion of eligible babies treated with dextrose gel from 1 month after implementation to 3 months after implementation) 6. Successful treatment with oral dextrose gel on the blood test taken immediately following dextrose gel treatment 7. Adherence to the 'oral dextrose gel to treat neonatal hypoglycaemia guideline' 8. Breastfeeding at discharge

Countries

New Zealand

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 25, 2026