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Clinical trialNCT00576693CompletedPhase 3Interventional

Stenting vs. Aggressive Medical Management for Preventing Recurrent Stroke in Intracranial Stenosis

SponsorMedical University of South CarolinaEnrollment451Ischemic Stroke
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

PRIMARY HYPOTHESIS: Compared with intensive medical therapy alone, intracranial angioplasty and stenting combined with intensive medical therapy will decrease the risk of the primary endpoint by 35% over a mean follow-up of two years in high-risk patients patients with 70% - 99% intracranial stenosis who had a transient ischemic attack (TIA) or stroke within 30 days prior to enrollment) with symptomatic stenosis of a major intracranial artery. SUMMARY: The best treatment for prevention of another stroke or TIA in patients with narrowing of one of the arteries in the brain is uncertain. A common treatment is the use of anti-clotting medications to prevent blood clots from forming in the narrowed vessel. There are a variety of medicines used for this purpose. These medications are usually taken for the rest of a patient's life. However, a treatment that has been used successfully together with anti-clotting medications in patients with narrowing of the blood vessels of the heart is now being studied in the blood vessels of the brain. This treatment is called stenting. Recent research has also indicated a benefit in prevention of recurring stroke by Intensive Medical Therapy, which is defined as treating risk factors for stroke like high blood pressure, elevated LDL (low density lipids - the "bad" form of cholesterol) and diabetes. The purpose of this study is to compare the safety and effectiveness of either Intensive Medical Therapy PLUS Stenting or Intensive Medical Therapy ONLY in preventing stroke, heart attacks or death. The study will enroll patients over a 5 year period. Each participant will be involved in the study for a minimum of 1 year and a maximum of 3 years. Fifty different medical centers in the United States are part of this study. Both the Clinical Coordinating Center and the Statistical Coordinating Center for the entire study will be located at Emory University.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

50 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Uab Medical Center

    Birmingham, Alabama, United States

  • Barrow Neurological Institute - St. Joseph'S Hospital and Medical Center

    Phoenix, Arizona, United States

  • Mayo

    Phoenix, Arizona, United States

  • Glendale Adventist

    Glendale, California, United States

  • Cedars Sinai

    Los Angeles, California, United States

  • Ucla

    Los Angeles, California, United States

  • Ucsf

    San Francisco, California, United States

  • Washington Hospital

    Washington D.C., District of Columbia, United States

  • University of Florida - Shands

    Gainesville, Florida, United States

  • University of Miami

    Miami, Florida, United States

  • Florida Hospital

    Winter Park, Florida, United States

  • Emory University

    Atlanta, Georgia, United States

  • Rush University Medical Center

    Chicago, Illinois, United States

  • Central Dupage Hospital

    Winfield, Illinois, United States

  • Johns Hopkins

    Baltimore, Maryland, United States

  • Massachusetts General Hospital

    Boston, Massachusetts, United States

  • Henry Ford Medical Center

    Detroit, Michigan, United States

  • Wayne State

    Detroit, Michigan, United States

  • Providence St. John

    Southfield, Michigan, United States

  • University of Mississippi

    Jackson, Mississippi, United States

  • University of Buffalo

    Buffalo, New York, United States

  • Columbia University Medical Center

    New York, New York, United States

  • Cornell Medical College

    New York, New York, United States

  • Nyu Medical Center

    New York, New York, United States

  • Stony Brook University Medical Center

    Stony Brook, New York, United States

  • Carolinas Medical Center

    Charlotte, North Carolina, United States

  • Duke University Medical Center

    Durham, North Carolina, United States

  • Moses Cone Medical Center

    Greensboro, North Carolina, United States

  • Forsyth Medical Center

    Winston-Salem, North Carolina, United States

  • University of Cincinnati

    Cincinnati, Ohio, United States

  • Cleveland Clinic

    Cleveland, Ohio, United States

  • University Hospitals Case Medical Center

    Cleveland, Ohio, United States

  • Riverside Methodist

    Columbus, Ohio, United States

  • Oregon Health Sciences University

    Portland, Oregon, United States

  • Thomas Jefferson University

    Philadelphia, Pennsylvania, United States

  • University of Pennsylvania

    Philadelphia, Pennsylvania, United States

  • University of Pittsburgh

    Pittsburgh, Pennsylvania, United States

  • Medical University of South Carolina

    Charleston, South Carolina, United States

  • Erlanger Medical Center

    Chattanooga, Tennessee, United States

  • Baylor University Medical Center

    Dallas, Texas, United States

10 more sites on the registry record.ClinicalTrials.gov ↗

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
31 Oct 2008
Primary completion
30 Apr 2013
Completion
30 Apr 2013
Last update posted
30 May 2018
Registered enrollment
451
Registry id
NCT00576693

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.