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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01192373
Other study ID # M20090230
Secondary ID
Status Completed
Phase Phase 2
First received August 24, 2010
Last updated January 18, 2013
Start date September 2010
Est. completion date March 2012

Study information

Verified date January 2013
Source University of Aarhus
Contact n/a
Is FDA regulated No
Health authority Denmark: The Regional Committee on Biomedical Research Ethics
Study type Interventional

Clinical Trial Summary

The investigators wish to investigate the the short term effect of low circulating free fatty acids in congestive heart failure patients with type 2 diabetes.

Hypothesis: Low levels of circulating free fatty acids decrease myocardial and peripheral muscle lipid content, improves cardiac performance and exercise capacity.


Recruitment information / eligibility

Status Completed
Enrollment 18
Est. completion date March 2012
Est. primary completion date March 2011
Accepts healthy volunteers No
Gender Both
Age group 30 Years to 85 Years
Eligibility Inclusion Criteria:

- ejection fraction at or lower than 45%

- type 2 diabetes

Exclusion Criteria:

- known s-creatinine >220mM

- known S-alanine aminotransferase >3 times normal upper limit

- other disabilitating conditions

- pregnancy

- insulin treatment

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Other:
Metabolic substrate modulation
for high circulation free fatty acids: Heparin (250IE/hour) + intralipid (20%, 62 ml/hour).
metabolic substrate modulation
low circulating free acids: hyperinsulinaemic euglycemic clamp (0,8 mUkg/min) with venous blood glucose at 4,5-6,5 mM.

Locations

Country Name City State
Denmark Dept. of cardiology, Aarhus University hospital Skejby, Aarhus Region Midjylland

Sponsors (2)

Lead Sponsor Collaborator
University of Aarhus Danish Heart Foundation

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Left ventricular function Left ventricular systolic function (Ejection fraction, tissue velocity, Strain and strain rate).
Left ventricular diastolic funtion (E/A ratio, E/e' ratio, IVRT) Cardiac output. All parameters measured at rest and peak exercise and outcome is difference between low and high ciculating free fatty acids.
1-6 weeks No
Primary intracellular lipid content Magnetic Resonans proton spectroscopy (septal myocardial intracellular lipid content) Magnetic Resonans proton spectroscopy (Tibialis anterior muscle intracellular lipid content).
Outcome is difference between low and high ciculating free fatty acids.
1-6 weeks No
Primary Exercise capacity and oxygen consumption Using treadmill and continues oxygen consumption measurement. Outcome is difference between low and high ciculating free fatty acids. 1-6 weeks No
Secondary Regional left ventricular function regional speckle tracking during rest and peak exercise. Outcome is difference between low and high ciculating free fatty acids. 1-6 weeks No
Secondary 6 minutes hall walk test distance difference between low and high levels of circulating FFA. Outcome is difference between low and high ciculating free fatty acids. 1-6 weeks No
Secondary metabolic and hormonal profile bloodsamples 1-6 weeks No
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