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Insulin Resistance Intervention After Stroke Trial (IRIS)
This study is currently recruiting participants.
Verified by National Institute of Neurological Disorders and Stroke (NINDS), December 2008
First Received: September 20, 2004   Last Updated: December 11, 2008   History of Changes
Sponsors and Collaborators: Yale University
National Institute of Neurological Disorders and Stroke (NINDS)
Information provided by: National Institute of Neurological Disorders and Stroke (NINDS)
ClinicalTrials.gov Identifier: NCT00091949
  Purpose

The purpose of this study is to determine if pioglitazone is effective in preventing future strokes or heart attacks among non-diabetic persons who have had a recent ischemic stroke.


Condition Intervention Phase
Stroke
Myocardial Infarction
Diabetes
Drug: pioglitazone
Drug: placebo
Phase III

MedlinePlus related topics: Diabetes Heart Attack
Drug Information available for: Insulin Pioglitazone Pioglitazone hydrochloride
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Double Blind (Subject, Investigator, Outcomes Assessor), Placebo Control, Parallel Assignment, Efficacy Study
Official Title: Insulin Resistance Intervention After Stroke (IRIS) Trial

Further study details as provided by National Institute of Neurological Disorders and Stroke (NINDS):

Primary Outcome Measures:
  • Time to occurrence of recurrent fatal or non-fatal stroke [ Time Frame: 3 years ] [ Designated as safety issue: No ]
  • fatal or non-fatal myocardial infarction. [ Time Frame: 3 years ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • 1.time to stroke alone; 2.Diabetes Mellitus; 3.All Cause Mortality; 4.Cognitive Decline (change in score over time for the Modified Mini Mental State Examination) [ Time Frame: 3 years ] [ Designated as safety issue: No ]
  • stroke, MI, or congestive heart failure [ Time Frame: 3 years ] [ Designated as safety issue: Yes ]

Estimated Enrollment: 3136
Study Start Date: February 2005
Estimated Study Completion Date: June 2009
Estimated Primary Completion Date: June 2009 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
1: Active Comparator
pioglitazone
Drug: pioglitazone
a thiazolidinedione drug
2: Placebo Comparator Drug: placebo
an inactive substance

Detailed Description:

Recurrent stroke and heart attack are major sources of illness and death among the 400,000 Americans who survive a stroke each year. Within 4 years of the initial stroke, 16 percent of patients will have a recurrent stroke and 9 percent will have a heart attack. Prevention of further vascular events, therefore, is critically important to the health of patients with stroke.

The IRIS trial will test a new treatment strategy based on evidence linking insulin resistance to increased risk for stroke and other vascular diseases.

Insulin resistance is a condition in which insulin, a normal human hormone, does not work effectively because the body is resistant to its effects.

This condition can lead to diabetes and is thought to cause blood vessel disease, including stroke and heart attack, in patients with and without diabetes.

Insulin resistance affects up to 50% of stroke patients and is effectively modified with thiazolidinedione drugs (called "TZDs") used to treat type 2 diabetes. In addition to reducing insulin resistance, these drugs have other favorable effects on blood vessels, reduce blood vessel inflammation, and potentially prevent atherosclerosis. Currently marketed TZDs include rosiglitazone and pioglitazone.

The IRIS is a clinical trial that will enroll 3136 subjects at approximately 100 hospitals in the US and Canada. After an initial screening blood test, each participant will be randomly assigned to take either pioglitazone or placebo tablets. Recruitment will be completed in 3 years, and all participants will be followed for a minimum of 3 years.

  Eligibility

Ages Eligible for Study:   40 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

To be eligible you must:

  • Be 40 years and older
  • Be non-diabetic
  • Have a recent transient ischemic attack or stroke
  • Be insulin resistant as determined by a special fasting blood test
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00091949

Contacts
Contact: Walter N. Kernan, M.D. 203-764-7000

  Show 108 Study Locations
Sponsors and Collaborators
Yale University
Investigators
Principal Investigator: Walter N. Kernan, M.D. Yale University
  More Information

No publications provided

Responsible Party: Yale University School of Medicine ( Walter N. Kernan, MD, Principal Investigator )
Study ID Numbers: R01NS044876, CRC
Study First Received: September 20, 2004
Last Updated: December 11, 2008
ClinicalTrials.gov Identifier: NCT00091949     History of Changes
Health Authority: United States: Food and Drug Administration

Keywords provided by National Institute of Neurological Disorders and Stroke (NINDS):
stroke
heart attack
diabetes
pioglitazone
insulin resistance

Study placed in the following topic categories:
Metabolic Diseases
Heart Diseases
Pioglitazone
Cerebral Infarction
Myocardial Ischemia
Stroke
Vascular Diseases
Diabetes Mellitus
2,4-thiazolidinedione
Central Nervous System Diseases
Ischemia
Brain Diseases
Cerebrovascular Disorders
Insulin
Hyperinsulinism
Necrosis
Hypoglycemic Agents
Brain Ischemia
Brain Infarction
Insulin Resistance
Infarction
Glucose Metabolism Disorders
Metabolic Disorder
Myocardial Infarction

Additional relevant MeSH terms:
Cerebral Infarction
Pioglitazone
Myocardial Ischemia
Physiological Effects of Drugs
Brain Diseases
Cerebrovascular Disorders
Insulin
Hyperinsulinism
Necrosis
Pathologic Processes
Hypoglycemic Agents
Brain Ischemia
Cardiovascular Diseases
Myocardial Infarction
Heart Diseases
Metabolic Diseases
Stroke
Nervous System Diseases
Vascular Diseases
Central Nervous System Diseases
Ischemia
Pharmacologic Actions
Insulin Resistance
Brain Infarction
Glucose Metabolism Disorders
Infarction

ClinicalTrials.gov processed this record on May 06, 2009