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ClinicalTrials.gov record
Active, not recruiting Phase 4 Interventional

Women's IschemiA TRial to Reduce Events In Non-ObstRuctive CAD

ClinicalTrials.gov ID: NCT03417388

Public ClinicalTrials.gov record NCT03417388. 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, 5:56 AM EDT

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

Brief summary

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

The Ischemia-IMT (Ischemia-Intensive Medical Treatment Reduces Events in Women with Non-Obstructive CAD), subtitle: Women's Ischemia Trial to Reduce Events in Non-Obstructive CAD (WARRIOR) trial is a multicenter, prospective, randomized, blinded outcome evaluation (PROBE design) evaluating intensive statin/ACE-I (or ARB)/aspirin treatment (IMT) vs. usual care (UC) in 4,422 symptomatic women patients with symptoms and/or signs of ischemia but no obstructive CAD. The hypothesis is that IMT will reduce major adverse coronary events (MACE) 20% vs. UC. The primary outcome is first occurrence of MACE as death, nonfatal MI, nonfatal stroke/transient ischemic attack (TIA) or hospitalization for heart failure or angina. Secondary outcomes include quality of life, time to "return to duty"/work, health resource consumption, angina, cardiovascular (CV) death and primary outcome components. Events will be adjudicated by an experienced Clinical Events Committee (CEC). Follow-up was planned to be 3-years using 50 sites: primarily VA and Active Duty Military Hospitals/Clinics and a National Patient-Centered Clinical Research Network (PCORnet) clinical data research network (CDRN)(OneFlorida Consortium). The number of sites were increased and follow up was modified to continue until the last patient enrolled was followed until trial follow up was completed. Recruitment was complete January 6, 2024. This study is being conducted to determine whether intensive medication treatment to modify risk factors and vascular function in women patients with coronary arteries showing no flow limit obstruction but with cardiac symptoms (i.e., chest pain, shortness of breath) will reduce the patient's likelihood of dying, having a heart attack, stroke/TIA or being hospitalized for cardiac reasons. The results will provide evidence data necessary to inform future guidelines regarding how best to treat this growing population of patients, and ultimately improve the patient's cardiac health and quality of life and reduce health-care costs.

Study identification

NCT ID
NCT03417388
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 4
Enrollment
2,476 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 100 Years
Sex
Female
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 9, 2018 (Actual)
Primary completion
Sep 14, 2026 (Estimated)
Completion
Sep 14, 2026 (Estimated)
Last update posted
May 29, 2026

2018 – 2026

United States locations

U.S. sites
80
U.S. states
25
U.S. cities
57
Facility City State ZIP Site status
Cardiology Associates of Mobile, Inc. Mobile Alabama 36608 —
Dignity Health-Mercy Gilbert Medical Center Gilbert Arizona 85297 —
Dignity Health-St. Joseph Phoenix Arizona 85013 —
University of Arizona Tucson Arizona 85721 —
University of Arkansas Little Rock Arkansas 72205 —
Cedars-Sinai Heart Institute Los Angeles California 90048 —
UCLA Medical Center Los Angeles California 90095 —
Lundquist Institute for Biomedical Innovation at Harbor UCLA Medical Center Torrance California 90502 —
Georgetown University Washington D.C. District of Columbia 20057 —
Clearwater Cardiovascular Consultants Clinical Research Clearwater Florida 33756 —
South Palm Cardiovascular Research Institute Delray Beach Florida 33446 —
Family Medicine at Eastside Community Practice Gainesville Florida 32206 —
Family Medicine at Hampton Oaks Medical Plaza (Adults and Peds) Gainesville Florida 32607 —
Internal Medicine at Tower Hill Gainesville Florida 32607 —
Family Medicine at Haile Plantation (Adults & Peds) Gainesville Florida 32608 —
Malcom Randall VA Medical Center Gainesville Florida 32608 —
Cardiovascular Clinic at UF Health UF Gainesville Florida 32610 —
Internal Medicine at UF Health Medical Plaza Gainesville Florida 32610 —
Spring Hill Cardiology Gainesville Florida 32610 —
Family Medicine at 4th Ave Gainesville Florida 32611 —
Family Medicine at Old Town (Adults and Peds) Gainesville Florida 32680 —
Baptist Health Jacksonville Florida 32207 —
University of Florida, Jacksonville Jacksonville Florida 32209 —
Naval Hospital Jacksonville Jacksonville Florida 32214 —
Mayo Clinic Jacksonville Jacksonville Florida 32224 —
UF Primary Care at Lake City SW Lake City Florida 32024 —
UF Primary Care at Lake City West Lake City Florida 32024 —
Charles H. Croft MDPA Melbourne Florida 32901 —
Daytona Heart Group Multiple Locations Florida 32114 —
Southwest Florida Research Institute Naples Florida 34102 —
Cardiovascular Instititute of Central Florida Ocala Florida 34471 —
Ocala Research Institute Inc. Ocala Florida 34480 —
Orlando Health Orlando Florida 32806 —
Naval Hospital Pensacola Pensacola Florida 32512 —
Cardiovascular Center of Sarasota Sarasota Florida 34239 —
Advent Sebring Sebring Florida 33872 —
James A. Haley Veterans Hospital Tampa Florida 33612 —
AdventHealth Tampa - Pepin Heart Institute Tampa Florida 33613 —
Interventional Cardiac Consultants Tampa Florida 33613 —
BayCare Medical Group Tampa Florida 33614 —
Guardian Research Winter Park Florida 32792 —
Emory University Atlanta Georgia 30322 —
Cardiovascular Consultants of South Georgia, LLC. Thomasville Georgia 31792 —
Loyola University Chicago Chicago Illinois 60660 —
Medicoricium Fairview Heights Illinois 62208 —
Carle Foundation Hospital Urbana Illinois 61801 —
Midwest Cardiovascular Research and Education Foundation Elkhart Indiana 46514 —
Lutheran Health Physicians Fort Wayne Indiana 46804 —
Midwest Heart and Vascular Specialists Overland Park Kansas 66211 —
Western Kentucky Heart And Lung Bowling Green Kentucky 42103 —
The Research Group of Lexington, LLC Lexington Kentucky 40503 —
University of Kentucky Lexington Kentucky 40506 —
Walter Reed National Military Medical Center Bethesda Maryland 20889 —
Berkshire Medical Center Pittsfield Massachusetts 01201 —
Mid Michigan Health Midland Michigan 48670 —
Essentia Institute of Rural Health Duluth Minnesota 55805 —
Minneapolis Heart Institute Foundation Minneapolis Minnesota 55407 —
Cardiology Associates Research, LLC Tupelo Mississippi 38801 —
Cardiology Associates Research. LLC Tupelo Mississippi 38801 —
CHI Health Research Center Omaha Nebraska 68124 —
Silver State Cardiology Henderson Nevada 89052 —
The Valley Hospital Ridgewood New Jersey 07450 —
Bassett Healthcare Network Cooperstown New York 13326 —
NYU Langone New York New York 10016 —
Weil Medical college of Cornell New York New York 10065 —
Jamaica Hospital Medical Center Richmond Hill New York 11418 —
Peak Clinical Trials, LLC Apex North Carolina 27502 —
Pinehurst Medical Clinic Pinehurst North Carolina 38274 —
The Christ Hospital Cincinnati Ohio 45219 —
Trihealth Heart Institute Cincinnati Ohio 45242 —
Heart House Research Foundation Springfield Ohio 45505 —
Seton Heart Institute Austin Texas 78705 —
Austin Heart Austin Texas 78756 —
Brooke Army Medical Center Fort Sam Houston Texas 78234 —
San Antonio Endovascular and Heart Institute San Antonio Texas 78258 —
Baylor Scott and White Temple Texas 76508 —
University of Virginia Health System Charlottesville Virginia 22908 —
Chippenham Hospital Richmond Virginia 23225 —
Carilion Clinic Roanoke Virginia 24017 —
West Virginia University Morgantown West Virginia 26508 —

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 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03417388, 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 May 29, 2026 · 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 NCT03417388 live on ClinicalTrials.gov.

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