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Completed Phase 4 Interventional Results available

Effect of Ranolazine on Myocardial Perfusion Assessed by Serial Quantitative Exercise SPECT Imaging

ClinicalTrials.gov ID: NCT01221272

Public ClinicalTrials.gov record NCT01221272. 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 3, 2026, 5:22 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

A Phase 4, Randomized, Double-Blind, Placebo-Controlled, Cross-over Trial to Evaluate the Effects of Ranolazine on Myocardial Perfusion Assessed by Serial Quantitative Exercise SPECT Imaging

Brief summary

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

This study enrolled participants with documented exercise-induced myocardial ischemia in order to evaluate whether ranolazine, when taken prior to exercise, can improve blood flow to the heart (myocardial perfusion), as assessed by exercise-induced myocardial perfusion defect size (PDS) and total perfusion deficit (TPD), using gated single photon emission computed tomography (SPECT) myocardial perfusion imaging (MPI). This was a 2-period crossover study. The last dose of each period must have been taken 3-4 hours prior to conduct of the exercise SPECT MPI. After the research exercise SPECT MPI was performed at the end of Period 1, participants discontinued the treatment they were randomized to for that period and began the other treatment in Period 2.

Study identification

NCT ID
NCT01221272
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Gilead Sciences
Industry
Enrollment
81 participants

Conditions and interventions

Interventions

Drug · Procedure · Behavioral

Eligibility (public fields only)

Age range
18 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
Aug 31, 2010
Primary completion
Aug 31, 2012
Completion
Aug 31, 2012
Last update posted
Sep 2, 2014

2010 – 2012

United States locations

U.S. sites
26
U.S. states
16
U.S. cities
26
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama 35294
Imperial Cardiac Center Imperial California 92251
Clinical Trials Research Lincoln California 95648
Mission Internal Medical Group Mission Viejo California 92691
Central Coast Cardiology Salinas California 93901
Alfieri Cardiology Newark Delaware 19713
St. Luke's Cardiology Associates Jacksonville Florida 32216
Cardiovascular Research Center of South Florida Miami Florida 33173
Research One Orlando Florida 32806
Cardiology Partners Clinical Research Institute Wellington Florida 33449
Fox Valley Clinical Research Center, LLC Aurora Illinois 60504
Research Integrity, LLC Owensboro Kentucky 42303
Louisiana Heart Center Covington Louisiana 70403
Louisiana Heart Center Slidell Louisiana 70458
Androscroggin Cardiology Associates DBA Maine Research Associates Auburn Maine 04210
Delmarva Heart Research Foundation, Inc Salisbury Maryland 21804
Massachusetts General Hospital Boston Massachusetts 02114
Cardiovascular Imaging Technologies Kansas City Missouri 64111
Dr. Michael Sacher Massapequa New York 11758
Columbia University Medical Center New York New York 10032
Duke University Medical Center Durham North Carolina 27710
Heritage Cardiology Camp Hill Pennsylvania 17011
University of Pittsburgh Medical Center Cardiovascular Institute Pittsburgh Pennsylvania 15213
Kore Cardiovascular Research Jackson Tennessee 38305
East Texas Cardiology PA Houston Texas 77002
Mercury Medical, LLC San Antonio Texas 78229

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 17 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01221272, 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 Sep 2, 2014 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01221272 live on ClinicalTrials.gov.

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