Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

Caffeine's Effect on Regadenoson Administration With Single Photon Emission Computed Tomography (SPECT) Myocardial Perfusion Imaging (MPI)

ClinicalTrials.gov ID: NCT00826280

Public ClinicalTrials.gov record NCT00826280. 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 Jul 22, 2026, 6:48 PM 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 3b, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Effect of Caffeine Intake on Single Photon Emission Computed Tomography (SPECT) Myocardial Perfusion Imaging (MPI) in Subjects Administered Regadenoson

Study identification

NCT ID
NCT00826280
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Astellas Pharma Inc
Industry
Enrollment
347 participants

Conditions and interventions

Interventions

  • regadenoson Drug
  • overencapsulated caffeine Drug
  • technetium Radiation
  • placebo Drug

Drug · Radiation

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
Mar 23, 2009
Primary completion
Jul 14, 2010
Completion
Jul 14, 2010
Last update posted
Dec 2, 2024

2009 – 2010

United States locations

U.S. sites
25
U.S. states
15
U.S. cities
25
Facility City State ZIP Site status
Not listed Birmingham Alabama 35294
Not listed Huntsville Alabama 35801
Not listed La Mesa California 91942
Not listed Mission Viejo California 92691
Not listed Roseville California 95661
Not listed Sacramento California 95819
Not listed Santa Rosa California 95405
Not listed Hartford Connecticut 06102-5037
Not listed Newark Delaware 19173
Not listed Jacksonville Florida 32216
Not listed Miami Florida 33173
Not listed Tamarac Florida 33321
Not listed Aurora Illinois 60504
Not listed Overland Park Kansas 66209
Not listed Auburn Maine 04210
Not listed Pittsfield Massachusetts 01201
Not listed Detroit Michigan 48202
Not listed Ypsilanti Michigan 48197
Not listed Kansas City Missouri 64111
Not listed Albany New York 12205
Not listed Rochester New York 14642-8679
Not listed Columbus Ohio 43214
Not listed Philadelphia Pennsylvania 19102
Not listed Wyomissing Pennsylvania 19610
Not listed Knoxville Tennessee 37920

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00826280, 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 Dec 2, 2024 · Synced Jul 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00826280 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →