Impaired Glucose Tolerance Clinical Trial
Official title:
Sucralose, Stevia, Gut Microbiome and Glucose Metabolism
Verified date | March 2018 |
Source | University of Minnesota - Clinical and Translational Science Institute |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study will determine the influence of two non-caloric sweeteners on glucose metabolism via the gut microbiome in adult men and women.
Status | Completed |
Enrollment | 40 |
Est. completion date | January 31, 2018 |
Est. primary completion date | January 31, 2018 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 35 Years to 55 Years |
Eligibility |
Inclusion Criteria: Generally health adult men and women aged 35-55 years old - Exclusion Criteria:Adults will not be eligible who have chronic disease (cancer, CHD, diabetes, chronic kidney disease); pregnant or breast feeding; menopausal; has a history of bariatric surgery; taking prednisone/steroids, taking medication for PCOS, or take medications that influence blood glucose. |
Country | Name | City | State |
---|---|---|---|
United States | ECRC | Minneapolis | Minnesota |
Lead Sponsor | Collaborator |
---|---|
University of Minnesota - Clinical and Translational Science Institute |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | 2-hour glucose | An oral glucose tolerance test will be administered before and after consuming assigned sweetener to determine change in 2-hour glucose | 14 days | |
Secondary | Gut microbiome | Gut microbiota will be measured before and after consuming assigned sweetener to determine change in gut microbiota. | 14 days |
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