Type 2 Diabetes Clinical Trial
NCT number | NCT02650830 |
Other study ID # | 4-2015-0503 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | September 12, 2015 |
Est. completion date | July 2, 2018 |
Verified date | January 2019 |
Source | Yonsei University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
"The goal of this work is to critically test the hypothesis that there exists a different
profile of bile acids (BAs) in patient with type 2 diabetes mellitus (T2DM) compared with
normal controls. Through confirmation of different profile of BAs in T2DM, investigator will
suggest modulation of specific bile acids as a new possible treatment target in patients with
T2DM. Investigator also expect the specific BAs signature will be used to screen T2DM before
hyperglycemia.
In addition, investigator will evaluate the association between each BA species and serum
total glucagon like peptide-1 (GLP-1) or fibroblast growth factor-19 (FGF-19) concentrations
to determine if the specific BAs profile is related with total GLP-1 or FGF-19 concentration
in serum. Investigatr also evaluates the correlation between each BA species and metabolic
profiles and oxidative stress marker to find possible roles of each BA component in glucose
metabolism.
Status | Completed |
Enrollment | 362 |
Est. completion date | July 2, 2018 |
Est. primary completion date | July 2, 2018 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 19 Years to 80 Years |
Eligibility |
Inclusion Criteria: 1. pre-diabetes 1. defined according to the ADA guideline (prediabetes definition) FPG 100 mg/dL (5.6 mmol/L) to 125 mg/dL (6.9 mmol/L) (IFG) or 2-h PG in the 75-g OGTT 140 mg/dL (7.8 mmol/L) to 199 mg/dL (11.0 mmol/L) (IGT) or A1C 5.7-6.4% (39-46 mmol/mol) 2. type 2 diabetes 1. defined according to the ADA guideline (DM definition) FPG =126 mg/dL (7.0 mmol/L) or 2-h PG =200 mg/dL (11.1 mmol/L) in the 75-g OGTT or A1C =6.5% (48 mmol/mol) or In a patient with classic symptoms of hyperglycemia or hyperglycemic crisis, a random plasma glucose =200 mg/dL (11.1 mmol/L) or 2. taking any anti-diabetic medications 3. Normal control 1. should not be included in other groups as above and 2. not taking any medication related to diabetes and dyslipidemia and 3. BMI <25kg/m2 Exclusion Criteria: 1. subjects who refused to agree with informed consents 2. subjects with organ-transplantation 3. pregnant women 4. type 1 diabetes - |
Country | Name | City | State |
---|---|---|---|
Korea, Republic of | Yonsei University College of Medicine | Seoul |
Lead Sponsor | Collaborator |
---|---|
Yonsei University |
Korea, Republic of,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | bile acid profile | Bile acids profile to predict T2DM will be measured using high performance liquid chromatography-tandem mass spectrometry. | 8h fasting blood sample |
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