Tiny sensor tracks blood sugar in preterm babies to boost brain health
NCT ID NCT05436925
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study placed a continuous glucose monitor (CGM) on 24 preterm infants born before 31 weeks to track their blood sugar levels for up to 10 days. The goal was to see how well the device detects high and low blood sugar, and to link those readings to the babies' growth and brain development over time. The CGM was used for research only, not to guide treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Dexcom G6 continuous glucose monitor (CGM)
- What this could lead to
- If successful, this could help doctors better manage blood sugar in preterm infants, potentially improving their growth and brain development.
- What could go wrong
- This is a small, early-stage study with only 24 infants, so results may not apply to all preterm babies. The CGM is used for research only, not for diagnosis.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
24 people
The number who actually took part.
- Started
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Oct 2022
- Finished
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Aug 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Preterm infants (gestational age (GA) at birth \<31 weeks) admitted to the University of Minnesota Masonic Children's Hospital
- Ages
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Up to 72 hours
- Sex
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Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * preterm infants (gestational age (GA) at birth \< 31 weeks) * admitted to the University of Minnesota Masonic Children's Hospital Neonatal Intensive Care Unit * written informed consent can be secured from a parent within 96 hours of birth. Exclusion Criteria: * Infants born at ≥31 weeks GA * infants with a prenatally diagnosed clinical or genetic condition (other than prematurity) that is known to affect growth rate, adiposity, or neurocognitive development * children experiencing severe birth asphyxia, * children enrolled in another nutritional study, * children likely to be transferred out of the NICU
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
University of Minnesota
Minneapolis, Minnesota, 55455, United States
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