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IRIS
Primary Investigator:
Madeleine Geraghty, MD

Description:
This study is designed to compare the study medication (pioglitazone) vs. a placebo for prevention of stroke and myocardial infarction (heart attack) in individuals who have recently had either an ischemic stroke or a transient ischemic attack.

Eligibility:
  • Ischemic stroke or TIA within prior six months.
  • Not on diabetic medication.
  • Able to give informed consent and participate in follow-up.
  • Insulin resistant (by IRIS blood test).
  • Other eligibility criteria may apply. Please contact study coordinator.

Exclusions:
  • Age < 45 years
  • Stroke or TIA due to structural cardiac lesion, trauma, dissection, or instrumentation
  • Class III or IV heart failure
  • Advanced liver disease
  • Limited life expectancy
  • Use of oral steroids or oral contraceptives
  • Pregnancy or intended pregnancy
  • Other exclusion criteria may apply. Please contact study coordinator.

Study Timeline:
Currently open to enrollment

Study Contact:
Ruthie, RN Ruth.Franks@providence.org

Study Sponsor:
National Institute of Neurological Disorders and Stroke




Keywords :
  • adult
  • CVA
  • Insulin resistant syndrome
  • IRIS
  • medication
  • prevention
  • stroke
  • TIA

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