Could looser blood sugar targets during labor protect babies from low blood sugar?
NCT ID NCT06643351
First seen Jun 24, 2026 · Last updated Aug 14, 2026 · Updated 2 times
Summary
This study looks at whether allowing a slightly higher blood sugar range (70-110 mg/dL) during labor in mothers with diabetes can reduce the number of newborns with low blood sugar. Researchers will compare this approach to standard care in 169 pregnant women planning a vaginal delivery. The main goal is to see if fewer babies have low blood sugar right after birth.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Insulin (intravenous) and glucose monitoring
- What this could lead to
- If successful, this could lead to a safer blood sugar management approach during labor, reducing the risk of low blood sugar in newborns.
- What could go wrong
- This is a small, single-center study. The results may not apply to all hospitals or patients, and the new target range might not lower newborn hypoglycemia as hoped.
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.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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169 people
The number who actually took part.
- Started
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Dec 2024
- Finished
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Jul 2026
- 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.
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Female participants only
- Healthy volunteers
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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: * Pregnant patients with Pre-gestational (Type 1 or Type 2) or Gestational Diabetes * Singleton Gestations * Greater than or equal to 35 weeks gestation * Planned for vaginal delivery at the University of Pittsburgh Medical Center Magee-Womens Hospital (UPMC MWH) Exclusion Criteria: * Major fetal anomalies anticipated to require NICU admission * Planned Cesarean delivery
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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
-
Magee-Women's Hospital of UPMC
Pittsburgh, Pennsylvania, 15213, United States
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