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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02130505
Other study ID # NL17100.101.07
Secondary ID
Status Completed
Phase N/A
First received April 21, 2014
Last updated May 1, 2014
Start date June 2007
Est. completion date June 2008

Study information

Verified date May 2014
Source Sint Franciscus Gasthuis
Contact n/a
Is FDA regulated No
Health authority Netherlands: The Central Committee on Research Involving Human Subjects (CCMO)
Study type Interventional

Clinical Trial Summary

In this study, we will investigate both inflammatory systems in healthy volunteers and patients with T2DM on insulin therapy and hyperlipidemia (both familial hyperlipidemia (FH) and familial combined hyperlipidemia (FCH)) during an OGTT.


Description:

Cardiovascular disease (CVD) is number one killer in the Netherlands. Insulin resistance and dyslipideima are the main causes of CVD. Recently, we have shown that there is an acute leukocyte activation after an oral glucose tolerance test (OGTT) in patients with newly-diagnosed diabets mellitus type 2 (T2DM). Leukocyte activation is an important and obligatory aspect in the process of atherosclerosis. Complement system is another important inflammatory component in atherosclerosis, which becomes activated in the postprandial phase.

In this study, we will investigate both inflammatory systems in healthy volunteers and patients with T2DM on insulin therapy and hyperlipidemia (both familial hyperlipidemia (FH) and familial combined hyperlipidemia (FCH)) during an OGTT.


Recruitment information / eligibility

Status Completed
Enrollment 51
Est. completion date June 2008
Est. primary completion date June 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 45 Years to 65 Years
Eligibility Inclusion Criteria:

- Provide written informed consent

- Aged 45-65 years

- BMI < 35 kg/m2

Exclusion Criteria:

- Emotionally and intellectually not capable to decide about participation in the study and the consequences of participation. Subjects who are not able to understand the patient information

- Diabetes mellitus treated with oral antidiabetic medicine

- Type 1 diabetes mellitus

- Peripheral artery and/or coronary disease

- Untreated hypertension

- Alcohol use > 2 units/day

- Aberrations in kidney, liver and thyroid function

- Use of any experimental medication within 6 months of the study

- The use of immunosuppressive drugs

Study Design

Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Intervention

Dietary Supplement:
OGTT
Oral glucose tolerance test (OGTT) with 75 g of oral anhydrous glucose

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Sint Franciscus Gasthuis

Outcome

Type Measure Description Time frame Safety issue
Primary Postprandial change in leukocyte activation Leukocyte activation is determined by flow cytometry, using fluorescent labelled antibodies: FITC-conjugated anti-CD66b and PE-conjugated anti-CD11b, expressed in mean fluorescence intensity in arbitrary units. The difference in postprandial response, expressed as area under the curve, between patients with T2DM, FCH and healthy controls is determined using ANOVA. area under the curve during 2 hours No
Secondary Correlation between chronic glycemia and leukocyte activation To assess whether chronic hyperglycemia (HbA1c) correlates with postprandial leukocyte activation, correlation between HbA1c and postprandial leukocyte activation (area under the curve) will be determined for the total study group. area under the curve during 2 hours No
Secondary Correlation between acute glycemia and leukocyte activation To assess whether acute hyperglycemia correlates with postprandial leukocyte activation, correlation between fasting glucose levels and postprandial leukocyte activation (area under the curve) will be determined for the total study group. area under the curve during 2 hours No
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