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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT03749889
Other study ID # 00002745
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date September 4, 2018
Est. completion date August 5, 2019

Study information

Verified date September 2019
Source State University of New York at Buffalo
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The overall purpose of this intervention study is to examine whether low-carbohydrate dietary intervention will prevent the development of gestational diabetes mellitus (GDM) in high-risk pregnant women. The results of this study should help further our understanding of how pregnant women can help prevent gestational diabetes mellitus. We hypothesize that a lower carbohydrate diet will prevent the development of GDM.


Recruitment information / eligibility

Status Terminated
Enrollment 11
Est. completion date August 5, 2019
Est. primary completion date August 5, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- 18 - 40 years old

- BMI > 30 and/or history of gestational diabetes mellitus

- Currently in first trimester of pregnancy with single fetus (e.g. not twins, triplets, etc.)

- Newborns of current participants

Exclusion Criteria:

- Diabetes (types 1 and 2)

- History of major chronic disease or blood clotting disorders (e.g., cancer, heart disease, kidney disease, hypertension)

- Known fetal anomaly

- History of eating disorders

- Current use of medications that affect appetite or insulin secretion/sensitivity (e.g. stimulants)

- Current use of illegal substances, antipsychotic or opioid substitution medications, alcohol, or tobacco

Study Design


Related Conditions & MeSH terms


Intervention

Other:
100 g carbs
Participants will be assigned a diet of 100g carbs max for the day
MyPlate
40-65% of daily intake is from carbohydrates

Locations

Country Name City State
United States SUNY Buffalo Buffalo New York

Sponsors (1)

Lead Sponsor Collaborator
State University of New York at Buffalo

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Birth Outcome Questionnaire Upon delivery of the baby, a birth outcome questionnaire will be collected which includes questions about the delivery and birth of the baby and a question about gestational diabetes. The answer to gestational diabetes or not will be the measure for the outcome. 24 months
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