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

NCT ID: NCT00569959

Last Updated: 2015-11-26

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2006-11-30

Study Completion Date

2007-06-30

Brief Summary

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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.

Detailed Description

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Conditions

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Diabetes Mellitus Normal Glucose Metabolism Hyperlipidemia

Study Design

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Intervention Model

CROSSOVER

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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Fasting

Group Type OTHER

fasting 12+ hours

Intervention Type OTHER

fasting 12+ hours

Non-fasting

Group Type OTHER

Non-fasting

Intervention Type OTHER

Non-fasting

Interventions

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fasting 12+ hours

fasting 12+ hours

Intervention Type OTHER

Non-fasting

Non-fasting

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Park Nicollet Health Services patients due for routine lipid measures

Exclusion Criteria

* Unwilling or unable to provide consent
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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HealthPartners Institute

OTHER

Sponsor Role lead

Principal Investigators

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William Richards, MD

Role: PRINCIPAL_INVESTIGATOR

Park Nicollet Health Services

Locations

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Park Nicollet Internal and Family Medicine Clinics

Minneapolis, Minnesota, United States

Site Status

Countries

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United States

Other Identifiers

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03363-05-A

Identifier Type: -

Identifier Source: org_study_id