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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 Sep 6, 2026, 1:14 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 8, 2018
Primary completion
Sep 13, 2026
Completion
Sep 13, 2026
Last update posted
May 28, 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 28, 2026 · Synced Sep 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03417388 live on ClinicalTrials.gov.

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