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Assessment of Non-Fasting vs. Fasting Lipid Measures in Diabetes Patients

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00569959
First Posted: December 10, 2007
Last Update Posted: November 26, 2015
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
HealthPartners Institute
December 6, 2007
December 10, 2007
November 26, 2015
November 2006
Not Provided
LDL-Cholesterol [ Time Frame: Fasting 12+ hours vs. Non-fasting ]
Same as current
Complete list of historical versions of study NCT00569959 on ClinicalTrials.gov Archive Site
Other lipid parameters [ Time Frame: Fasting 12+ hours vs. non-fasting ]
Same as current
Not Provided
Not Provided
 
Assessment of Non-Fasting vs. Fasting Lipid Measures in Diabetes Patients
Assessment of Non-Fasting vs. Fasting Lipid Measures in Diabetes Patients
This study will examine whether fasting and non-fasting lipid measures can provide similar clinical information in order to guide lipid management by primary physicians. It will compare fasting vs. non-fasting lipid measurements in patients with and without diabetes.
Not Provided
Interventional
Not Provided
Intervention Model: Crossover Assignment
Masking: None (Open Label)
Primary Purpose: Diagnostic
  • Diabetes Mellitus
  • Normal Glucose Metabolism
  • Hyperlipidemia
  • Other: fasting 12+ hours
    fasting 12+ hours
  • Other: Non-fasting
    Non-fasting
  • Fasting
    Intervention: Other: fasting 12+ hours
  • Non-fasting
    Intervention: Other: Non-fasting
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
50
June 2007
Not Provided

Inclusion Criteria:

  • Park Nicollet Health Services patients due for routine lipid measures

Exclusion Criteria:

  • Unwilling or unable to provide consent
Sexes Eligible for Study: All
18 Years and older   (Adult, Senior)
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT00569959
03363-05-A
No
Not Provided
Not Provided
Not Provided
HealthPartners Institute
Not Provided
Principal Investigator: William Richards, MD Park Nicollet Health Services
HealthPartners Institute
December 2008

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP