Personalized meals for gestational diabetes? small study tests the idea
NCT ID NCT04187521
First seen Jun 27, 2026 ยท Last updated Jun 27, 2026
Summary
This study looked at whether women with different types of gestational diabetes respond differently to meals with varying amounts of carbs, protein, and fat. Nineteen women with gestational diabetes wore a continuous glucose monitor and ate two test meals. The goal was to see if matching meal plans to a woman's specific diabetes subtype could help control blood sugar better.
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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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19 people
The number who actually took part.
- Started
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Feb 2020
- Finished
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Nov 2022
- 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 years and older
- 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: -Diagnosis of gestational diabetes Exclusion Criteria: * Known diabetes mellitus that preceded pregnancy * Food allergies to components of the test meals * Use of medications known to affect glucose tolerance * Have extensive skin changes or diseases making CGM sensor use problematic * Demonstrated allergy to CGM adhesive * Inability to adhere to the swimming and bathing instructions * Plan to have MRI, CT scan, X Ray or diathermy (heat treatment) during the 7-day CGM study period * Inability to adhere to Vitamin C guidelines during study period (using more than 500 mg of Vitamin C/day which could interfere with the CGM) * Use of medications known to affect glucose tolerance * In the opinion of the principal investigator (PI), demonstrate any other factor likely to limit compliance with the protocol
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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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Brigham and Women's Hospital
Boston, Massachusetts, 02215, United States
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Massachusetts General Hospital
Boston, Massachusetts, 02114, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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