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The Usefulness of Postprandial Triglyceride for Assessment of Cardiovascular Risk

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Seoul National University

Status

Completed

Conditions

Prediabetes
Diabetes

Treatments

Dietary Supplement: Oral fat tolerance test

Study type

Interventional

Funder types

Other

Identifiers

NCT01972542
SNUBH-ENDO4

Details and patient eligibility

About

The hypertriglyceridemia at fasting status has been known to be an important risk factor for cardiovascular disease (CVD). Recently, postprandial triglyceride (TG) levels draw an attention as a superior predictor of CVD because of non-fasting state for more than 12 hours and importance of triglyceride-rich lipoprotein.

We aim to investigate the relationship of postprandial triglyceride after fat tolerance test and intima-medial thickness and to suggest normal reference of postprandial triglyceride after fat tolerance test. In addition, we evaluate the correlation of postprandial triglyceride and incretin secretion after fat tolerance test Ultimately, we want to estimate clinical importance of postprandial triglyceride in assessment of cardiovascular risk.

Enrollment

80 patients

Sex

All

Ages

19 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • age : 19 ~ 70 yrs
  • Type 2 diabetes : HbA1c <10%
  • Prediabetic state : HbA1c 5.7~6.4%

Exclusion criteria

  • Type 1 diabetes, secondary diabetes
  • dipeptidyl peptidase-4 -inhibitor, glucagon-like peptide-1 agonist, thiazolidinediones users
  • Thyroid disease with abnormal thyroid function test
  • Liver disease with abnormal liver function test
  • severe kidney disease
  • pregnant or lactating women
  • current smoker
  • severe obesity

Trial design

Primary purpose

Screening

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

80 participants in 3 patient groups

Type 2 DM
Active Comparator group
Description:
Intervention : Oral fat tolerance test well or moderately controlled type 2 diabetes mellitus (HbA1c \< 10%) No dipeptidyl peptidase-4 -inhibitor, Glucagon-like peptide-1 agonist, thiazolidinediones
Treatment:
Dietary Supplement: Oral fat tolerance test
Prediabetes
Active Comparator group
Description:
Intervention : Oral fat tolerance test Glucose 140-199 mg/dL after 75g oral glucose tolerance test HbA1c 5.7-6.4%
Treatment:
Dietary Supplement: Oral fat tolerance test
Normal glucose tolerance
Sham Comparator group
Description:
Intervention : Oral fat tolerance test No impaired fasting glucose and impaired glucose tolerance
Treatment:
Dietary Supplement: Oral fat tolerance test

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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