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Effect of Thiazolidinedione Treatment Vascular Risk Markers

Primary Purpose

Diabetes Mellitus, Type 2, Vascular Diseases

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Rosiglitazone
Pioglitazone
Sponsored by
University of Arkansas
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Mellitus, Type 2 focused on measuring Diabetes Mellitus, Type 2, Vascular Diseases, Thiazolidinediones, Platelet Aggregation

Eligibility Criteria

40 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Men and women of all races
  • Age 40-65 years
  • Diagnosis of type 2 diabetes
  • hemoglobin A1C ≥ 7%
  • eligible whether or not currently taking antihyperglycemic medications

Exclusion Criteria:

  • History of rosiglitazone or pioglitazone use in the previous 3 months
  • Known diagnosis of peripheral vascular disease or cardiac failure
  • Recent history (within past 6 months) of ischemic stroke, myocardial infarction, percutaneous coronary intervention, or coronary artery bypass surgery
  • Active liver disease or elevated serum transaminases (ALT >2.5x upper limit of normal)
  • Current therapy with oral anticoagulants (warfarin, heparin, low molecular weight heparin), clopidogrel, or immunosuppressive agents
  • Pregnancy or breastfeeding
  • Any other condition, in the opinion of the investigator, that renders the subject unable to complete the study, that interferes with optimal participation in the study, or that produces significant risk to the subject

Sites / Locations

  • University of Arkansas for Medical Sciences

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

1

2

Arm Description

Rosiglitazone 4 mg by mouth daily

Pioglitazone 30 mg by mouth daily

Outcomes

Primary Outcome Measures

determine if treatment with rosiglitazone or pioglitazone affects platelet function as assessed by spontaneous and agonist-induced platelet aggregation

Secondary Outcome Measures

adipocytokine concentrations (adiponectin, leptin), hemostatic parameters (fibrinogen, plasminogen activator inhibitor-1), high-sensitivity C-reactive protein

Full Information

First Posted
December 10, 2007
Last Updated
December 8, 2009
Sponsor
University of Arkansas
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1. Study Identification

Unique Protocol Identification Number
NCT00571506
Brief Title
Effect of Thiazolidinedione Treatment Vascular Risk Markers
Official Title
A Pilot Study to Determine the Effects of Short-term Thiazolidinedione Treatment on Vascular Risk Markers in Type 2 Diabetes Patients
Study Type
Interventional

2. Study Status

Record Verification Date
December 2009
Overall Recruitment Status
Completed
Study Start Date
May 2004 (undefined)
Primary Completion Date
August 2007 (Actual)
Study Completion Date
August 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
University of Arkansas

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to examine the effects of two diabetes medications, rosiglitazone and pioglitazone, on markers of vascular disease in subjects with type 2 diabetes.
Detailed Description
Diabetes is a common disease in the United States, affecting over 10 million Americans. Vascular disease, including heart attack and stroke, affects many diabetic patients and will cause the death of three-fourths of these patients. Because the majority of diabetic patients will suffer complications or death from vascular disease, we will explore treatments that have the potential to reduce or prevent vascular disease in type 2 diabetes patients. Our study will examine the effects of two diabetes medications, rosiglitazone (ROSI) and pioglitazone (PIO), on markers of vascular disease in 20 subjects with type 2 diabetes. It is thought that these two medications will reduce the risk of vascular disease by affecting the platelets and proteins that that regulate the processes involved in clot formation. One-half of the subjects enrolled in our study will take ROSI and the other half will take PIO. We will measure the clumping ability of these subjects' platelets before, during, and after three months of treatment with ROSI or PIO. We will measure the blood concentrations of several proteins (fibrinogen, PAI-1, CRP, adiponectin, and leptin) before and after treatment with the study drugs. These experiments will give us information about any beneficial effects of ROSI and PIO on the clot-forming ability in diabetes patients. We expect that treatment with ROSI and PIO will result in improvement of the disturbed clot-forming processes that predispose diabetic patients to vascular disease.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 2, Vascular Diseases
Keywords
Diabetes Mellitus, Type 2, Vascular Diseases, Thiazolidinediones, Platelet Aggregation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
25 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Rosiglitazone 4 mg by mouth daily
Arm Title
2
Arm Type
Active Comparator
Arm Description
Pioglitazone 30 mg by mouth daily
Intervention Type
Drug
Intervention Name(s)
Rosiglitazone
Other Intervention Name(s)
Avandia
Intervention Description
Rosiglitazone 4 mg tablets by mouth daily for 3 months
Intervention Type
Drug
Intervention Name(s)
Pioglitazone
Other Intervention Name(s)
Actos
Intervention Description
Pioglitazone 30 mg tablet by mouth once daily
Primary Outcome Measure Information:
Title
determine if treatment with rosiglitazone or pioglitazone affects platelet function as assessed by spontaneous and agonist-induced platelet aggregation
Time Frame
3 months
Secondary Outcome Measure Information:
Title
adipocytokine concentrations (adiponectin, leptin), hemostatic parameters (fibrinogen, plasminogen activator inhibitor-1), high-sensitivity C-reactive protein
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Men and women of all races Age 40-65 years Diagnosis of type 2 diabetes hemoglobin A1C ≥ 7% eligible whether or not currently taking antihyperglycemic medications Exclusion Criteria: History of rosiglitazone or pioglitazone use in the previous 3 months Known diagnosis of peripheral vascular disease or cardiac failure Recent history (within past 6 months) of ischemic stroke, myocardial infarction, percutaneous coronary intervention, or coronary artery bypass surgery Active liver disease or elevated serum transaminases (ALT >2.5x upper limit of normal) Current therapy with oral anticoagulants (warfarin, heparin, low molecular weight heparin), clopidogrel, or immunosuppressive agents Pregnancy or breastfeeding Any other condition, in the opinion of the investigator, that renders the subject unable to complete the study, that interferes with optimal participation in the study, or that produces significant risk to the subject
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Amy M. Franks, Pharm.D.
Organizational Affiliation
University of Arkansas
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Arkansas for Medical Sciences
City
Little Rock
State/Province
Arkansas
ZIP/Postal Code
72205
Country
United States

12. IPD Sharing Statement

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Effect of Thiazolidinedione Treatment Vascular Risk Markers

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