Dyslipidemia in Type 2 Diabetes (0767-034)

NCT ID: NCT00547274

Last Updated: 2015-06-12

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

TERMINATED

Clinical Phase

PHASE3

Total Enrollment

111 participants

Study Classification

INTERVENTIONAL

Study Start Date

2003-07-31

Study Completion Date

2003-11-30

Brief Summary

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The purpose of the study is to compare the lipid-altering effects of MK0767, glipizide, and pioglitazone after 12 weeks of treatment.

This is an early phase trial and some specific protocol information is in progress and not publicly available at this time. (Full information is available to trial participants).

Detailed Description

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Conditions

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Diabetes Mellitus, Type II Dyslipidemia

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Investigators

Interventions

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MK0767

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Men and non-pregnant females
* Age greater than or equal to 21 years
* Stop current diabetes therapy (if applicable)
* Stop current statin therapy (if applicable)

Exclusion Criteria

* History of type 1 diabetes mellitus or ketoacidosis who are currently being treated with insulin
* Patients on a weight loss program with ongoing weight loss, or starting an intensive exercise program within the last four weeks
* Patients requiring treatment with corticosteroids for more than 14 consecutive days
* Patients taking warfarin or warfarin-like anti-coagulants
* Patients undergoing surgery within 30 days of Visit 1
* Patients with Hepatitis B, Hepatitis C, active liver or gallbladder disease
* Patients with history of pancreatitis or uncontrolled high blood pressure
Minimum Eligible Age

21 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Merck Sharp & Dohme LLC

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Medical Monitor

Role: STUDY_DIRECTOR

Merck Sharp & Dohme LLC

Other Identifiers

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2007_635

Identifier Type: -

Identifier Source: secondary_id

MK-0767-034

Identifier Type: -

Identifier Source: secondary_id

0767-034

Identifier Type: -

Identifier Source: org_study_id

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