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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01024543
Other study ID # MEC 06-2-074
Secondary ID
Status Completed
Phase N/A
First received November 30, 2009
Last updated December 1, 2009
Start date October 2006
Est. completion date November 2009

Study information

Verified date December 2009
Source Maastricht University Medical Center
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 hypothesize infusion of Angiotensin II improves the insulin-induced microvascular dilatation and therefore insulin-mediated glucose uptake. Objectives: Does infusion of Angiotensin II increase insulin-mediated glucose uptake via enhanced insulin-mediated microvascular function in healthy subjects?


Recruitment information / eligibility

Status Completed
Enrollment 18
Est. completion date November 2009
Est. primary completion date November 2009
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

1.18-60 years 2.Caucasian 3.Blood pressure <140/90 mmHg.

Exclusion Criteria:

1. Obesity (BMI>27kg/m2)

2. Cardiovascular disease (stroke, coronary artery disease, peripheral vascular disease, heart failure)

3. Impaired glucose tolerance or 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

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Basic Science


Related Conditions & MeSH terms


Intervention

Drug:
Angiotensin II
Angiotensin II
Phenylephrine
Phenylephrine
Placebo


Locations

Country Name City State
Netherlands Maastricht University Medical Centre Maastricht, P.o. Box 5800, Netherlands

Sponsors (1)

Lead Sponsor Collaborator
Maastricht University Medical Center

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary functional recruitment of capillaries in the skin January 2009 No
Secondary perfused capillary density in the nailfold January 2009 No
Secondary Endothelium- (in)dependent vasodilatation of finger skin microcirculation January 2006 No
Secondary Insulin sensitivity January 2009 No
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