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Is Milk Associated with Glycemia in the NICU

Is Milk Associated with Glycemia in the NICU (MAGIC) a Study in the NICU

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05256927
Acronym
MAGIC
Enrollment
124
Registered
2022-02-25
Start date
2022-02-16
Completion date
2024-03-10
Last updated
2025-03-10

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

Conditions

Premature Birth

Brief summary

The purpose of this study is to determine if concentrations of hormones in prepared human milk (HM) feeds are associated with metabolic disturbances in the recipient premature infant. To do so, prospectively 100 infants receiving HM-derived fortifiers as part of clinical care will be studied, saving aliquots of daily prepared feeds until any fortification ceases.

Detailed description

The purpose of this study is to determine if concentrations of these hormones in prepared HM feeds are associated with metabolic disturbances in the recipient infant. A prospectively study 100 infants receiving HM-derived fortifiers as part of clinical care, saving aliquots of daily prepared feeds until any fortification ceases. Insulin and PTHrP will be compared in feeds from matched days when metabolic disturbances were documented vs not; each infant serving as a control. Hypothesis 1 Feed dose of insulin and PTHrP will be higher from days when hypoglycemia and hypercalcemia are observed, respectively, vs control days when metabolic disturbances are not observed. Hypothesis 2: Over time, daily feed dose of insulin will correlate with average daily blood glucose in infants receiving HM products.

Interventions

None listed

Sponsors

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
CollaboratorNIH
University of Rochester
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
0 Days to 3 Months
Healthy volunteers
No

Inclusion criteria

* Infants eligible to receive human milk (HM)-derived fortifiers. To qualify for these fortifiers, infants must be born \<30 weeks gestation and/or weigh \<1250g at birth. Enteral or oral feeding modes both qualify for participation. Additional supplementation to feeds beyond HM-derived fortifier (such as medium-chain triglycerides) is acceptable. * Infants initially on intravenous nutrition will still be eligible for consent. Feed sample collections from these infants will commence once they advance to consume HM-based feeds once HM-derived fortifier is prescribed.

Exclusion criteria

* Infants diagnosed with congenital disorders that impact glucose or calcium metabolism will be excluded. * Infants with conditions necessitating specialized diets (ex: chylothorax) will also be excluded. * Non-English speaking subjects will be excluded as the team of study personnel includes those that speak English only.

Design outcomes

Primary

MeasureTime frameDescription
Insulin concentration in prepared feeds3 monthsWe will measure final insulin concentrations in enteral feed preparations that contain some portion of human milk.
Parathyroid hormone related protein (PTHrP) concentration in prepared feeds3 monthsWe will measure final PTHrP concentrations in enteral feed preparations that contain some portion of human milk.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026