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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
  Purpose
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.

Condition Intervention
Diabetes Mellitus Normal Glucose Metabolism Hyperlipidemia Other: fasting 12+ hours Other: Non-fasting

Study Type: Interventional
Study Design: Intervention Model: Crossover Assignment
Masking: None (Open Label)
Primary Purpose: Diagnostic
Official Title: Assessment of Non-Fasting vs. Fasting Lipid Measures in Diabetes Patients

Further study details as provided by HealthPartners Institute:

Primary Outcome Measures:
  • LDL-Cholesterol [ Time Frame: Fasting 12+ hours vs. Non-fasting ]

Secondary Outcome Measures:
  • Other lipid parameters [ Time Frame: Fasting 12+ hours vs. non-fasting ]

Enrollment: 50
Study Start Date: November 2006
Study Completion Date: June 2007
Arms Assigned Interventions
Fasting Other: fasting 12+ hours
fasting 12+ hours
Non-fasting Other: Non-fasting
Non-fasting

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Park Nicollet Health Services patients due for routine lipid measures

Exclusion Criteria:

  • Unwilling or unable to provide consent
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00569959


Locations
United States, Minnesota
Park Nicollet Internal and Family Medicine Clinics
Minneapolis, Minnesota, United States, 55416
Sponsors and Collaborators
HealthPartners Institute
Investigators
Principal Investigator: William Richards, MD Park Nicollet Health Services
  More Information

ClinicalTrials.gov Identifier: NCT00569959     History of Changes
Other Study ID Numbers: 03363-05-A
First Submitted: December 6, 2007
First Posted: December 10, 2007
Last Update Posted: November 26, 2015
Last Verified: December 2008

Keywords provided by HealthPartners Institute:
fasting lipid measures
non-fasting lipid measures
clinical decision-making
LDL-Cholesterol

Additional relevant MeSH terms:
Diabetes Mellitus
Hyperlipidemias
Hyperlipoproteinemias
Glucose Metabolism Disorders
Metabolic Diseases
Endocrine System Diseases
Dyslipidemias
Lipid Metabolism Disorders