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Blood Glucose in Pregnant Non-diabetic Women During Treatment With Betamethasone for Fetal Lung Maturation

Recruitingn/aAges 18 Years - anyFemaleUniversity of Aarhus
NCT06794307 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

In case of threatening preterm birth, it is standard to recommend treatment with betamethasone to accelerate fetal lung maturation. In pregnant women with diabetes, treatment with betamethasone can lead to significant hyperglycemia, which may cause hypoglycemia in the neonate. Changes in blood glucose in non-diabetic women are less investigated. In this study we aim to examine changes in maternal blood glucose levels in non-diabetic women, during treatment with betamethasone, by continuous glucose monitoring. Hypotheses: Administration of betamethasone induce significant hyperglycemia in non-diabetic pregnant women during treatment.

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📋 Eligibility rules (as published)
Inclusion Criteria: * Pregnant in gestational week 24+0 - 34+0 admitted with symptoms of threatened preterm birth: * Premature contractions and shortening of the cervix, or * Preterm premature rupture of membranes. * Treatment with betamethasone for fetal lung maturation is planned, or started (maximum 4 hours before inclusion) * Age over 18 years * Read and understand Danish Exclusion Criteria: * Multiple pregnancy * Diabetes * Pre-existing maternal use of medications that affect glucose metabolism
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What it tests

  • Not listed
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Where

1 site
Aarhus University Hospital
Aarhus, Denmark
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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