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Microvascular Dilatation After Endogenous Induced Hyperinsulinemia

Insulin-induced Microvascular Dilatation During a Physiological Stimulus - Studies in Hypertension and Obesity.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00742456
Enrollment
48
Registered
2008-08-27
Start date
2009-01-31
Completion date
2010-08-31
Last updated
2011-02-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertension, Obesity

Keywords

Microcirculation, Insulin, Hypertension, Obesity

Brief summary

In this study we will examine if the insulin-induced microvascular effects will occur after a physiological stimulus (i.e. a oral glucose tolerance test). With that the physiological importance of the insulin-induced microvascular dilatation can be elucidated. In this study we hypothesize that oral glucose intake and consequently the endogenous induced hyperinsulinemia will lead to insulin-induced microvascular dilatation in healthy normotensive subjects. Furthermore, we suggest that the insulin-mediated microvascular dilatation, resulting from this physiological induced hyperinsulinemia, will be less in hypertensive and obese subjects compared to healthy controls.

Interventions

DIETARY_SUPPLEMENTGlucose solution

single oral intake of 250 ml glucose solution (75gr sugar in 250ml of water)

DIETARY_SUPPLEMENTPlacebo

single intake of placebo solution (250ml of sweet flavored water, no sugar added), orally

Sponsors

Maastricht University Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

healthy normotensive subjects: 1. 18-60 years 2. Caucasian 3. Blood pressure \<140/90 mmHg obese normotensive subjects: 1. 18-60 years 2. Caucasian 3. Blood pressure \<140/90 mmHg 4. BMI 30-38kg/m2 hypertensive subjects: 1. 18-60 years 2. Caucasian 3. Untreated hypertension \>140/90mmHg.

Exclusion criteria

for healthy normotensive and hypertensive subjects: 1. Obesity (BMI\>27kg/m2) 2. Cardiovascular disease (stroke, coronary artery disease, peripheral vascular disease, heart failure) 3. Diabetes mellitus according to the criteria of the ADA 4. Smoking 5. Alcohol use \>4U/day 6. Use of medication (antihypertensive drugs, lipid lowering drugs, corticosteroids, NNSAIDs) 7. Pregnancy 8. Wearing contact lenses for normotensive obese subjects: 1. Cardiovascular disease (stroke, coronary artery disease, peripheral vascular disease, heart failure) 2. Impaired glucose tolerance or diabetes mellitus according to the criteria of the ADA 3. Smoking 4. Alcohol use \>4U/day 5. Use of medication (antihypertensive drugs, lipid lowering drugs, corticosteroids, NNSAIDs) 6. Pregnancy 7. Wearing contact lenses

Design outcomes

Primary

MeasureTime frame
Functional recruitment of capillaries in the skin.January 2009 - January 2010

Secondary

MeasureTime frame
Perfused capillary density in the nailfold.January 2009 - January 2010
Endothelium- (in)dependent vasodilatation of finger skin microcirculationJanuary 2009 - January 2010
Density of arterioles, capillaries and venules in the bulbar conjunctiva.January 2009 - January 2010
Diameter of arterioles and venules in the bulbar conjunctiva.January 2009 - January 2010
Insulin sensitivity (HOMA-IR)January 2009 - January 2010

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026