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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01178957
Other study ID # ES-0004
Secondary ID
Status Completed
Phase N/A
First received April 21, 2010
Last updated August 5, 2013
Start date April 2012
Est. completion date April 2013

Study information

Verified date August 2013
Source University of Aarhus
Contact n/a
Is FDA regulated No
Health authority Denmark: Danish Dataprotection Agency
Study type Observational

Clinical Trial Summary

The purpose of this study is to estimate the acute effect of hyperglycemia on Very-Low-Density-Lipoprotein-triglyceride(VLDL-TG) secretion.


Recruitment information / eligibility

Status Completed
Enrollment 8
Est. completion date April 2013
Est. primary completion date April 2013
Accepts healthy volunteers No
Gender Male
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

1. Type 1 diabetes

2. Age 18-50 years

Exclusion Criteria:

1. Smoking

2. Alcohol abuse

3. Use of medications (except insulin in diabetics)

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Other:
Hyperglycemia
Hyperglycemia with a blood glucose of 15 mmol/L

Locations

Country Name City State
Denmark Department of Endocrinology MEA, Aarhus Hospital Aarhus C

Sponsors (1)

Lead Sponsor Collaborator
University of Aarhus

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Very-Low-Density-Lipoprotein-Triglyceride(VLDL-TG) secretion Very-Low-Density-Lipoprotein-Triglyceride(VLDL-TG) kinetics over a single study day 8 hours No
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