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A Randomised Controlled Trial of Pasteurised Donor Human Milk as Supplementary Nutrition for Infants Born to Women With Diabetes in Pregnancy.

Status: Recruiting
Location: See all (4) locations...
Intervention Type: Dietary supplement, Other
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

PRESENT is a multi-center randomised controlled trial that aims to assess whether access to pasteurized donor human milk as supplementary nutrition in the first five days of life for term infants born to women with diabetes in pregnancy reduces the proportion of infants who are admitted to a neonatal unit for management of hypoglycemia compared with current standard hospital care. The trial will also assess other important outcomes including breastfeeding rates, maternal mental health, and infant cow's milk allergy. There will be two treatment arms. In the intervention arm, PDHM will be made available to infants from randomisation until day 5 of life. Infants allocated to the control arm will receive care as per local unit policy, including supplemental nutrition as recommended by the treating clinician. After hospital discharge, participants will be asked to complete an electronic questionnaire at 2 \& 6 weeks and 6 \& 12 months after birth. Questionnaires will assess infant feeding practices, maternal quality of life \[including anxiety and depression symptoms and health-related quality of life\] along with infant cow's milk allergy symptoms.

Eligibility
Participation Requirements
Sex: All
Maximum Age: 2 days
Healthy Volunteers: f
View:

⁃ Each participant must meet all the following criteria to be enrolled in this trial:

• Mother is \>18 years at the time of consent

• Mother has diabetes in pregnancy (type 1, type 2 or gestational diabetes)

• Mother intends to breastfeed for at least 6 weeks at the time of consent.

• Infant is born at ≥ 37 weeks and weighs \> 2.5kg

• Clinician caring for infant decides that supplementary nutrition (in addition to maternal breast milk) is required within the first 48 hours after birth.

• Parent/s provide/s a signed and dated informed consent form and has a legally acceptable representative capable of understanding the informed consent document and providing consent on the participant's behalf.

Locations
Other Locations
Australia
Greenslope Hospital (QLD)
NOT_YET_RECRUITING
Brisbane
Royal Brisbane and Womens Hospital (QLD)
NOT_YET_RECRUITING
Brisbane
Frances Perry House (VIC)
NOT_YET_RECRUITING
Melbourne
Royal Womens Hospital (VIC)
RECRUITING
Melbourne
Contact Information
Primary
Jennifer Koplin, PhD
j.koplin@uq.edu.au
061+0400032577
Backup
Vanessa Clifford, PhD
VClifford@redcrossblood.org.au
061+0437 527 044
Time Frame
Start Date: 2025-12-04
Estimated Completion Date: 2028-12
Participants
Target number of participants: 1444
Treatments
Experimental: PDHM - Pasteurised donor human milk
All infants in this group will get access to Pasteurised donor human milk (PDHM) as supplementary nutrition. PDHM will be made available to the intervention group from the time of randomisation until day 5 of life. Families will be provided with a sufficient supply of frozen PDHM for home use to ensure an exclusively human milk diet up to day 5 of life if their infant is discharged before day 5. Access to PDHM will cease after 120 hours of life, and the infant will be fed according to standard hospital protocols or as per parent's decision.
Active_comparator: Standard Care
All infants in this group will receive the standard care as per local unit policy, including supplemental nutrition (e.g. infant cow's milk formula or IV fluids) as recommended by the treating clinician
Sponsors
Collaborators: Monash University, The Royal Women Hospital, Murdoch Childrens Research Institute, Ramsay Hospital Research Foundation, La Trobe University, Australian Red Cross Lifeblood, Frances Perry House (Ramsay Health), South Australian Health and Medical Research Institute, University of Melbourne
Leads: The University of Queensland

This content was sourced from clinicaltrials.gov

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