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Inflammation and Insulin Resistance in Rheumatoid Arthritis

Primary Purpose

Rheumatoid Arthritis

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Pioglitazone
Placebo
Sponsored by
Vanderbilt University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Rheumatoid Arthritis focused on measuring RA, Rheumatoid Arthritis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Meets the American College of Rheumatology (ACR) criteria for the diagnosis of rheumatoid arthritis (RA)
  • Stable disease activity, as evidenced by no change in immunomodulating or anti-inflammatory therapy in the 1 month before study entry
  • Moderate disease activity, as reflected by a minimum of three swollen and tender joints
  • If female of childbearing potential, willing to use effective method of contraception

Exclusion Criteria:

  • Allergic to pioglitazone
  • Active cancer (other than skin cancer)
  • HIV infected
  • Currently receiving dialysis
  • Received an organ or bone marrow transplant
  • Heart failure
  • Severe edema, as judged by the principal investigator
  • Diabetes mellitus requiring drug therapy: levels of aspartate aminotransferase (AST) or alanine aminotransferase (ALT) greater than twice the upper limit of normal
  • Underwent major surgery in the 3 months before study entry
  • Severe comorbid condition that is likely to compromise survival or study participation
  • Currently receiving gemfibrozil or rifampin
  • Osteoporosis and not receiving osteoporosis medications
  • Unwillingness, or other inability, to cooperate with study procedures
  • Pregnancy

Sites / Locations

  • Vanderbilt Clinical Research Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Placebo First

Pioglitazone First

Arm Description

Placebo for first 8 weeks, then washout period for 4 weeks, and finally pioglitazone for 8 weeks.

Pioglitazone for first 8 weeks, then washout period for 4 weeks, and finally placebo for 8 weeks.

Outcomes

Primary Outcome Measures

Disease Activity Score Based on 28-joint Disease Activity Score (DAS28)
A measure of disease activity based upon tender joint count of 28 joints, swollen joint count of 28 joints, erythrocyte sedimentation rate, and global disease activity (GH) as reported by participant. Calculation is as follows: DAS28=0.56*sqrt(t28) + 0.28*sqrt(sw28) + 0.70*Ln(ESR) + 0.014*GH
Homeostasis Model Assessment (HOMA) for Insulin Sensitivity
Homa is a measure of insulin sensitivity, using glucose measured in mmol/L and insulin measured in milliUnits per liter (mU/L) Calculated using the formula Glucose * Insulin/22/5

Secondary Outcome Measures

C-reactive Protein (CRP)
ESR
sed rate

Full Information

First Posted
September 26, 2008
Last Updated
November 12, 2014
Sponsor
Vanderbilt University
Collaborators
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
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1. Study Identification

Unique Protocol Identification Number
NCT00763139
Brief Title
Inflammation and Insulin Resistance in Rheumatoid Arthritis
Official Title
Inflammation and Insulin Resistance in Rheumatoid Arthritis
Study Type
Interventional

2. Study Status

Record Verification Date
November 2014
Overall Recruitment Status
Completed
Study Start Date
April 2009 (undefined)
Primary Completion Date
September 2012 (Actual)
Study Completion Date
December 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Vanderbilt University
Collaborators
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Rheumatoid arthritis (RA) is a form of arthritis that causes pain, swelling, stiffness, and loss of function in the joints. Over time, joint deformity, joint destruction, and loss of function can occur. Current treatment aims to improve symptoms, but there is no cure for the disease. Pioglitazone is drug that is effective in treating people with diabetes. This study will determine whether pioglitazone can also be used to effectively treat people with RA.
Detailed Description
RA is an autoimmune disease that causes long-term inflammation of the joints and sometimes other body tissues, too. Recent studies have found that there is an increased prevalence of coronary artery atherosclerosis, metabolic syndrome, and insulin resistance among people with RA. Furthermore, insulin resistance, which can lead to hyperinsulinemia-too much insulin in the blood-has been associated with RA disease activity and the severity of coronary artery atherosclerosis. These correlations suggest that inflammation and hyperinsulinemia somehow interact and facilitate one another. Pioglitazone is a prescription drug that reduces insulin resistance and is currently used to treat people with diabetes. This study will determine whether pioglitazone can also be used to effectively treat people with RA. Specifically, the study will evaluate the effect of pioglitazone on inflammation, insulin resistance, and atherosclerosis. Participation in this study will last about 20 weeks. At an initial 1-hour screening, participants will undergo a physical examination, medical history review, blood sampling, and, if female, a urine pregnancy test. Eligible participants will then return for the first of six monthly study visits. At this first visit, participants will be randomly assigned to receive either pioglitazone or placebo, both of which will be taken daily for 8 weeks. This will be followed by a 4-week wash-out period, during which no study treatments will be taken. Then, at Week 12, participants will begin daily treatments of whatever they were not assigned to originally. This second treatment phase will also last for 8 weeks. All of the study visits will involve the same tests and procedures. The morning before each study visit, participants will collect their urine in a jug, which they will bring to the clinic. Participants will then undergo blood sampling, blood pressure measurements, and artery stiffness measurements. During the study visits at Weeks 4, 8, 16, and 20, participants will be asked to report on their symptoms, pain, and any adverse effects.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rheumatoid Arthritis
Keywords
RA, Rheumatoid Arthritis

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
34 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Placebo First
Arm Type
Experimental
Arm Description
Placebo for first 8 weeks, then washout period for 4 weeks, and finally pioglitazone for 8 weeks.
Arm Title
Pioglitazone First
Arm Type
Experimental
Arm Description
Pioglitazone for first 8 weeks, then washout period for 4 weeks, and finally placebo for 8 weeks.
Intervention Type
Drug
Intervention Name(s)
Pioglitazone
Other Intervention Name(s)
Actos
Intervention Description
45 mg by mouth once a day for 8 weeks
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
By mouth once a day for 8 weeks
Primary Outcome Measure Information:
Title
Disease Activity Score Based on 28-joint Disease Activity Score (DAS28)
Description
A measure of disease activity based upon tender joint count of 28 joints, swollen joint count of 28 joints, erythrocyte sedimentation rate, and global disease activity (GH) as reported by participant. Calculation is as follows: DAS28=0.56*sqrt(t28) + 0.28*sqrt(sw28) + 0.70*Ln(ESR) + 0.014*GH
Time Frame
Measured after 8 weeks of treatment
Title
Homeostasis Model Assessment (HOMA) for Insulin Sensitivity
Description
Homa is a measure of insulin sensitivity, using glucose measured in mmol/L and insulin measured in milliUnits per liter (mU/L) Calculated using the formula Glucose * Insulin/22/5
Time Frame
Measured after 8 weeks of treatment
Secondary Outcome Measure Information:
Title
C-reactive Protein (CRP)
Time Frame
Measured after 8 weeks of treatment
Title
ESR
Description
sed rate
Time Frame
baseline and after 8 weeks on either placebo or pioglitazone

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Meets the American College of Rheumatology (ACR) criteria for the diagnosis of rheumatoid arthritis (RA) Stable disease activity, as evidenced by no change in immunomodulating or anti-inflammatory therapy in the 1 month before study entry Moderate disease activity, as reflected by a minimum of three swollen and tender joints If female of childbearing potential, willing to use effective method of contraception Exclusion Criteria: Allergic to pioglitazone Active cancer (other than skin cancer) HIV infected Currently receiving dialysis Received an organ or bone marrow transplant Heart failure Severe edema, as judged by the principal investigator Diabetes mellitus requiring drug therapy: levels of aspartate aminotransferase (AST) or alanine aminotransferase (ALT) greater than twice the upper limit of normal Underwent major surgery in the 3 months before study entry Severe comorbid condition that is likely to compromise survival or study participation Currently receiving gemfibrozil or rifampin Osteoporosis and not receiving osteoporosis medications Unwillingness, or other inability, to cooperate with study procedures Pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Charles M. Stein, MD
Organizational Affiliation
Vanderbilt University Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Vanderbilt Clinical Research Center
City
Nashville
State/Province
Tennessee
ZIP/Postal Code
37232-2195
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
24020899
Citation
Ormseth MJ, Oeser AM, Cunningham A, Bian A, Shintani A, Solus J, Tanner S, Stein CM. Peroxisome proliferator-activated receptor gamma agonist effect on rheumatoid arthritis: a randomized controlled trial. Arthritis Res Ther. 2013;15(5):R110. doi: 10.1186/ar4290.
Results Reference
result
PubMed Identifier
24782291
Citation
Ormseth MJ, Oeser AM, Cunningham A, Bian A, Shintani A, Solus J, Tanner SB, Stein CM. Reversing vascular dysfunction in rheumatoid arthritis: improved augmentation index but not endothelial function with peroxisome proliferator-activated receptor gamma agonist therapy. Arthritis Rheumatol. 2014 Sep;66(9):2331-8. doi: 10.1002/art.38686.
Results Reference
derived

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Inflammation and Insulin Resistance in Rheumatoid Arthritis

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