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

This study has been completed.
Sponsor:
Information provided by:
Park Nicollet Institute
ClinicalTrials.gov Identifier:
NCT00569959
First received: December 6, 2007
Last updated: January 5, 2009
Last verified: December 2008
  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: Open Label
Primary Purpose: Diagnostic
Official Title: Assessment of Non-Fasting vs. Fasting Lipid Measures in Diabetes Patients

Resource links provided by NLM:


Further study details as provided by Park Nicollet 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

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
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
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00569959

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

No publications provided

ClinicalTrials.gov Identifier: NCT00569959     History of Changes
Other Study ID Numbers: 03363-05-A
Study First Received: December 6, 2007
Last Updated: January 5, 2009
Health Authority: United States: Institutional Review Board

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

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

ClinicalTrials.gov processed this record on August 01, 2014