Comparison of two medicines in heartr perfusion stress studies.

• Conditions: Coronary artery desease; MedDRA version: 14.1Level: PTClassification code 10011078Term: Coronary artery diseaseSystem Organ Class: 10007541 - Cardiac disorders; Therapeutic area: Diseases [C] - Cardiovascular Diseases [C14]

• Registration Number: EUCTR2013-001225-11-FI
• Lead Sponsor: Turku University Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2013-05-13
• Last Update Posted: 27 January 2014

Recruitment & Eligibility

• Status: Authorised-recruitment may be ongoing or finished
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

One of the following:
Age 18-80
Suspected CAD and referred for cardiac PET perfusion imaging based on clinical indications
Known CAD and referred for cardiac PET perfusion imaging based on clinical indications
Patients have been or are referred for coronary angiography, either noninvasive or invasive
Informed consent from the patient

Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 8
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range 7

Exclusion Criteria

Continuing, uncontrolled unstable angina symptoms or urgent CABG after invasive coronary angiography
ST-elevation myocardial infarction (STEMI)
EF < 40% or diagnosis of cardiomyopathy
Prior coronary artery bypass grafting (CABG)
Haemophilia, Von Willebrand's disease or other coagulation disorder
Severe pulmonary disease
Symptomatic asthma
Severe valvular disease
Uncontrolled hypertension (>180/110 mmHg)
Moderate to severe renal failure
Women with childbearing potential
Age < 18 or > 80 years
Unstable asthma
II or III degree AV block or sick sinus syndrome without pacemaker
Severe hypotension (systolic bloodpressure < 90 mmHg),
Allergy to x-ray contrast agents (patients have also angiography)

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified