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Completed Phase 3 Interventional

Secondary Prevention of Small Subcortical Strokes Trial

ClinicalTrials.gov ID: NCT00059306

Public ClinicalTrials.gov record NCT00059306. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 9:49 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Secondary Prevention of Small Subcortical Strokes (SPS3) Trial

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The goal of this study is to learn if combination antiplatelet therapy (aspirin and clopidogrel) is more effective than aspirin alone for the prevention of recurrent stroke and cognitive decline, and if intensive blood pressure control is associated with fewer recurrent strokes and cognitive decline. On July 21, 2011 the DSMB recommended terminating the anti platelet arm of the study due to an imbalance of overall and major non-CNS hemorrhagic SAE's and total deaths in the investigational anti platelet combination of aspirin + clopidogrel and an interim statistical analysis that demonstrated futility in the investigational anti platelet arm. It was recommended that patients be continued on standard care of aspirin mono therapy until their study close-out visit. Also, recommended the continuation and completion of the plood pressure arm following the protocol.

Study identification

NCT ID
NCT00059306
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
3,020 participants

Conditions and interventions

Eligibility (public fields only)

Age range
30 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 2003 (Type not available)
Primary completion
Apr 2012 (Actual)
Completion
Apr 2012 (Actual)
Last update posted
Apr 4, 2013

2003 – 2012

United States locations

U.S. sites
39
U.S. states
22
U.S. cities
35
Facility City State ZIP Site status
University of Southern Alabama Stroke Center Mobile Alabama 36617 —
Catholic Healthcare West Phoenix Arizona 85013 —
Mayo Clinic Scottsdale Scottsdale Arizona 85259 —
University of Arizona, Department of Neurology Tucson Arizona 85724 —
University of California San Diego Medical Center San Diego California 92103-8466 —
University of California San Francisco-Fresno San Francisco-Fresno California — —
Denver Englewood Colorado — —
Melbourne Melbourne Florida — —
Miami-University of Miami, Miller School of Medicine Miami Florida 33136 —
Emory University, Grady Health System Atlanta Georgia 30303 —
Mercy Medical Center-Ruan Neurology Clinical Research Des Moines Iowa 50314 —
University of Kentucky, Aging/Stroke Program Lexington Kentucky 40506-0230 —
Suburban Hospital Bethesda Maryland — —
Boston University Boston Massachusetts 02118 —
Wayne State Detroit Michigan 48201 —
Henry Ford Hospital, Department of Neurology Detroit Michigan 48202 —
Berman Center Minneapolis Minnesota 55404 —
Mayo Stroke Center KA-SL-13 Rochester Minnesota 55905 —
University of Washington Sant Louis Missouri — —
Tenet Health, St. Louis University St Louis Missouri 63110 —
St. John's Mercy St Louis Missouri 63141 —
Cooper University Hospital Camden New Jersey 08103 —
Buffalo Buffalo New York — —
Helen Hayes Hospital Haverstraw New York 10993 —
Columbia University Medical Center New York New York 10032 —
Rochester General Hospital Rochester New York 14621 —
University of Rochester Rochester New York 14642 —
Wake Forest University, Sciences-Neurology Winston-Salem North Carolina 27157-1078 —
Case Western Cleveland Ohio 44106 —
Metrohealth Medical Center Cleveland Ohio 44109 —
Ohio State University, Division of Stroke Columbus Ohio 43210 —
Oregon Health and Science University Portland Oregon 97239 —
Vanderbilt University Medical Center Nashville Tennessee 37232 —
University of Texas Southwestern Dallas Texas 75390-8897 —
Scurlock Stroke Center Houston Texas 77030 —
University of Texas Health Science Center San Antonio Texas 78229-3900 —
University of Washington Seattle Washington 98104-2499 —
Marshfield Clinic, Department of Neurology Marshfield Wisconsin 54449 —
Medical College of Wisconsin-Neurology Milwaukee Wisconsin 53226 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 24 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00059306, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 4, 2013 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00059306 live on ClinicalTrials.gov.

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