New York, New York 10025

  • Ischemic Heart Disease

Purpose:

The primary purpose of this study is to determine the optimal time for myocardial perfusion imaging with Technetium Tc99m Sestamibi following the administration of BMS068645. The safety of BMS068645 will also be studied.


Criteria:

Inclusion Criteria: - 18 years of age or older - Have known or suspected heart disease - Have undergone a clinically indicated SPECT MPI study with adenosine in the last 24 hours to 14 days. - Weigh between 88 and 250 lbs. Exclusion Criteria: - Allergic reaction to Technetium Tc99m Sestamibi or any of its components - History of asthma or lung disease - Ingestion of caffeinated substances within 12 hours prior to the study


NCT ID:

NCT00162071


Primary Contact:

Principal Investigator
E Gordon DePuey, MD
St. Luke's-Roosevelt Hospital Center


Backup Contact:

N/A


Location Contact:

New York, New York 10025
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: March 30, 2020

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