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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03331432
Other study ID # 1203573
Secondary ID
Status Completed
Phase N/A
First received October 26, 2017
Last updated February 14, 2018
Start date October 28, 2015
Est. completion date February 14, 2018

Study information

Verified date October 2017
Source University of Missouri-Columbia
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the present study is to determine if use of dietary supplement tauroursodeoxycholic acid enhances insulin-stimulated leg blood flow and glucose disposal.


Description:

The notion that cellular stress lowers insulin-induced vasodilation is largely founded on ex vivo studies and experiments in rodents. However, it remains unknown if maintenance of cellular function with the use of dietary supplement tauroursodeoxycholic acid enhances vascular function in humans. The investigators test the hypothesis that daily administration of this dietary supplement enhances vascular function, particularly, insulin-stimulated leg blood flow and glucose disposal.


Recruitment information / eligibility

Status Completed
Enrollment 8
Est. completion date February 14, 2018
Est. primary completion date August 15, 2017
Accepts healthy volunteers No
Gender All
Age group 20 Years to 65 Years
Eligibility Inclusion Criteria:

- Type 2 diabetes diagnosed by primary physician

- Body mass index less then 43 kg/m2

Exclusion Criteria:

- Recent weight gain or loss (>5% body weight in the last 3 months)

- Pregnancy

- Consumption of >14 alcoholic beverages per week

- Changes in the medication use or dose within the last 3 months

- Known cardiovascular or pulmonary disease

- Taking medication for advanced retinopathy or neuropathy

- Taking prescription anticoagulants

- Nicotine use

Study Design


Intervention

Dietary Supplement:
Tauroursodeoxycholic acid
Taking tauroursodeoxycholic acid (1750 mg/day) capsules for 4 weeks.
Placebo
Taking daily placebo capsules for 4 weeks.

Locations

Country Name City State
United States University of Missouri Columbia Missouri

Sponsors (1)

Lead Sponsor Collaborator
University of Missouri-Columbia

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Blood flow Blood flow response during insulin clamp Once at 4 weeks after the start of placebo and once at 4 weeks after the start of tauroursodeoxycholic acid
Primary Vascular function Flow-mediated dilation Once at 4 weeks after the start of placebo and once at 4 weeks after the start of tauroursodeoxycholic acid
Primary Insulin resistance Glucose disposal rate during insulin clamp Once at 4 weeks after the start of placebo and once at 4 weeks after the start of tauroursodeoxycholic acid
Primary Glucose tolerance Glucose response to an oral glucose tolerance test Once at 4 weeks after the start of placebo and once at 4 weeks after the start of tauroursodeoxycholic acid
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