New study tests High-Tech glucose monitors for pregnant women with diabetes
NCT ID NCT05370612
First seen Jun 27, 2026 ยท Last updated Jun 27, 2026
Summary
This study looked at whether using a continuous glucose monitor (CGM) is better than standard finger-prick checks for managing blood sugar in pregnant women with type 2 diabetes. Sixteen women participated, and researchers measured how well blood sugar stayed in a healthy range and how satisfied the women were with their diabetes care. The goal was to see if CGM is practical and helpful for this group.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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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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16 people
The number who actually took part.
- Started
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Aug 2022
- Finished
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Oct 2024
- 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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18 to 45 years
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age greater than or equal to 18 years of age at enrollment * Ability to consent in English * Gestational age less than or equal to 19 weeks 6 days at enrollment * Appropriate dating by certain LMP or ultrasound performed less than or equal to 19 weeks 6 day * Diagnosis of Type 2 Diabetes less than or equal to 19 weeks 6 days * Singleton gestation Exclusion Criteria: * Age less than 18 years of age at enrollment * Lack of appropriate dating * Multiple gestations * Use of concentrated insulin at enrollment (ie U500) * Preexisting CGM in place * Chronic use of medications known to cause hyperglycemia, such as HIV antiretrovirals and inhaled, injectable and oral corticosteroids * Be unwilling or unable to present to Center for Perinatal Care for visits
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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
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University of Wisconsin
Madison, Wisconsin, 53715, United States
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Other studies related to the condition(s) this trial covers.
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