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OpenTrials
Completed

NCT Number: NCT00569959

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.

Completed

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Key information

Conditions

Diabetes Mellitus Dyslipidemias Endocrine System Diseases Glucose Metabolism Disorders Hyperlipidemia Hyperlipidemias Lipid Metabolism Disorders Metabolic Diseases Normal Glucose Metabolism Nutritional and Metabolic Diseases

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Park Nicollet Internal and Family Medicine Clinics

Minneapolis, Minnesota, 55416, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Park Nicollet Health Services patients due for routine lipid measures

Exclusion criteria

  • Unwilling or unable to provide consent

Treatment and study plan

fasting 12+ hours

Other

fasting 12+ hours

Non-fasting

Other

Non-fasting

Primary outcomes

  1. LDL-Cholesterol

    Time frame: Fasting 12+ hours vs. Non-fasting

Secondary outcomes

  1. Other lipid parameters

    Time frame: Fasting 12+ hours vs. non-fasting

Sponsors and collaborators

Lead sponsor

HealthPartners Institute

Other

Registry information

Important dates

Study start
2006
Study completion
2007
First posted
Dec 10, 2007
Registry last updated
Nov 26, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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