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Clinical Trials/NCT00569959
NCT00569959CompletedNot Applicable

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

HealthPartners Institute2 sites in 1 country50 target enrollmentStarted: November 2006Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
50
Locations
2
Primary Endpoint
LDL-Cholesterol

Study Overview

Brief Summary

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.

Study Design

Study Type
Interventional
Intervention Model
Crossover
Primary Purpose
Diagnostic
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Park Nicollet Health Services patients due for routine lipid measures

Exclusion Criteria

  • Unwilling or unable to provide consent

Outcomes

Primary Outcomes

LDL-Cholesterol

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

Secondary Outcomes

  • Other lipid parameters(Fasting 12+ hours vs. non-fasting)

Investigators

Sponsor Class
Other

Study Sites (2)

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