Please note that the copy function is not enabled for this field.
If you wish to
modify
existing outcomes, please copy and paste the current outcome text into the Update field.
LOGIN
CREATE ACCOUNT
LOGIN
CREATE ACCOUNT
MY TRIALS
REGISTER TRIAL
FAQs
HINTS AND TIPS
DEFINITIONS
Trial Review
The ANZCTR website will be unavailable from 1pm until 3pm (AEDT) on Wednesday the 30th of October for website maintenance. Please be sure to log out of the system in order to avoid any loss of data.
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been endorsed by the ANZCTR. Before participating in a study, talk to your health care provider and refer to this
information for consumers
Download to PDF
Trial registered on ANZCTR
Registration number
ACTRN12606000343505
Ethics application status
Approved
Date submitted
30/03/2006
Date registered
11/08/2006
Date last updated
4/04/2008
Type of registration
Retrospectively registered
Titles & IDs
Public title
CHAMPION PCI
Query!
Scientific title
A Clinical trial comparing Cangrelor
to Clopidogrel in subjects who require percutaneous coronary intervention (PCI) to demonstrate that cangrelor is superior, or at least non-inferior, to that of clopidogrel as measured by a composite of all-cause mortality, myocardial infarction (MI) and ischaemia driven revascularisation (IDR).
Query!
Universal Trial Number (UTN)
Query!
Trial acronym
CHAMPION PCI
Query!
Linked study record
Query!
Health condition
Health condition(s) or problem(s) studied:
Unstable Angina
1312
0
Query!
Myocardial Infarction
1313
0
Query!
Acute Coronary Syndromes
1314
0
Query!
Condition category
Condition code
Cardiovascular
1399
1399
0
0
Query!
Other cardiovascular diseases
Query!
Intervention/exposure
Study type
Interventional
Query!
Description of intervention(s) / exposure
Subjects who fulfill the criteria and are to under go PCI will be randomised on a 1:1 randomisation to receive either 4 placebo capsules orally plus Cangrelor bolus (30ug/kg) & infusion (4 ug/kg/min) for at least 2 hours or the duration of the procedure, whichever is longer. Post infusion be administered 4 Clopidogrel capsules (600mg) orally once. The other group would receive 4 Clopidogrel capsules (600mg) plus Placebo bolus (30 ug/kg) and infusion (4 ug/kg/min) for the duration of the procedure or 2 hours whichever is longer. At the end of the infusion they will receive 4 placebo capsules once. Clopidogrel maintenance is at the physicians discretion.
Query!
Intervention code [1]
964
0
Treatment: Drugs
Query!
Comparator / control treatment
Placebo
Query!
Control group
Active
Query!
Outcomes
Primary outcome [1]
1914
0
All cause mortality
Query!
Assessment method [1]
1914
0
Query!
Timepoint [1]
1914
0
In the 48 hours after randomisation
Query!
Primary outcome [2]
1915
0
Myocardial Infaction
Query!
Assessment method [2]
1915
0
Query!
Timepoint [2]
1915
0
In the 48 hours after randomisation
Query!
Primary outcome [3]
1916
0
Ischaemic driven revascularization
Query!
Assessment method [3]
1916
0
Query!
Timepoint [3]
1916
0
In the 48 hours after randomisation
Query!
Secondary outcome [1]
3373
0
All cause mortality and myocardial infarction
Query!
Assessment method [1]
3373
0
Query!
Timepoint [1]
3373
0
At 30 days.
Query!
Eligibility
Key inclusion criteria
Diagnostic coronary angiography demonstrating atherosclerosis amenable to treatment by PCI with or without stent implantation and one of the following:
1. Non ST segment myocardial infarction with Troponin I or T greater than upper limit of normal within 24 hours of randomisation.
2. Unstable angina with ischaemic chest discomfort occurring at rest and lasting longer than 10 minutes within 24 hours of randomisation and with dynamic ECG changes with age greater than 65 years or diabetes.
Query!
Minimum age
18
Years
Query!
Query!
Maximum age
Not stated
Query!
Query!
Sex
Both males and females
Query!
Can healthy volunteers participate?
No
Query!
Key exclusion criteria
Glycoprotein IIb/IIIa (GPI) Inhibitor usuage within the previous 12 hours.
Query!
Study design
Purpose of the study
Treatment
Query!
Allocation to intervention
Randomised controlled trial
Query!
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Central randomisation by phone/fax
Query!
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Simple randomisation by using a randomisation table created by a computer software(ie computerised sequence generation).
Query!
Masking / blinding
Blinded (masking used)
Query!
Who is / are masked / blinded?
Query!
Query!
Query!
Query!
Intervention assignment
Parallel
Query!
Other design features
Active control
Query!
Phase
Phase 3
Query!
Type of endpoint/s
Safety/efficacy
Query!
Statistical methods / analysis
Query!
Recruitment
Recruitment status
Recruiting
Query!
Date of first participant enrolment
Anticipated
23/05/2006
Query!
Actual
Query!
Date of last participant enrolment
Anticipated
Query!
Actual
Query!
Date of last data collection
Anticipated
Query!
Actual
Query!
Sample size
Target
9000
Query!
Accrual to date
Query!
Final
Query!
Recruitment in Australia
Recruitment state(s)
Query!
Funding & Sponsors
Funding source category [1]
1533
0
Commercial sector/Industry
Query!
Name [1]
1533
0
The Medicines Company
Query!
Address [1]
1533
0
8 Campus Drive
Parsippany, NJ 07054
Query!
Country [1]
1533
0
United States of America
Query!
Primary sponsor type
Commercial sector/Industry
Query!
Name
The Medicines Company
Query!
Address
8 Campus Drive
Parsippany, NJ 07054
Query!
Country
United States of America
Query!
Secondary sponsor category [1]
1347
0
Hospital
Query!
Name [1]
1347
0
Flinders Medical Centre
Query!
Address [1]
1347
0
1 Flinders Drive
Bedford Park SA 5042
Query!
Country [1]
1347
0
Australia
Query!
Ethics approval
Ethics application status
Approved
Query!
Ethics committee name [1]
2956
0
Flinders Medical Centre
Query!
Ethics committee address [1]
2956
0
Query!
Ethics committee country [1]
2956
0
Australia
Query!
Date submitted for ethics approval [1]
2956
0
Query!
Approval date [1]
2956
0
Query!
Ethics approval number [1]
2956
0
TMC-CAN-05-02
Query!
Ethics committee name [2]
2957
0
Royal Adelaide Hospital
Query!
Ethics committee address [2]
2957
0
Query!
Ethics committee country [2]
2957
0
Australia
Query!
Date submitted for ethics approval [2]
2957
0
Query!
Approval date [2]
2957
0
Query!
Ethics approval number [2]
2957
0
TMC-CAN-05-02
Query!
Ethics committee name [3]
2958
0
The Queen Elizabeth Hospital
Query!
Ethics committee address [3]
2958
0
Query!
Ethics committee country [3]
2958
0
Australia
Query!
Date submitted for ethics approval [3]
2958
0
Query!
Approval date [3]
2958
0
Query!
Ethics approval number [3]
2958
0
TMC-CAN-05-02
Query!
Ethics committee name [4]
2959
0
Holy Spirit Hospital
Query!
Ethics committee address [4]
2959
0
Query!
Ethics committee country [4]
2959
0
Australia
Query!
Date submitted for ethics approval [4]
2959
0
Query!
Approval date [4]
2959
0
Query!
Ethics approval number [4]
2959
0
TMC-CAN-05-02
Query!
Ethics committee name [5]
2960
0
The Canberra Hospital
Query!
Ethics committee address [5]
2960
0
Query!
Ethics committee country [5]
2960
0
Australia
Query!
Date submitted for ethics approval [5]
2960
0
Query!
Approval date [5]
2960
0
Query!
Ethics approval number [5]
2960
0
TMC-CAN-05-02
Query!
Ethics committee name [6]
2961
0
Royal Brisbane
Query!
Ethics committee address [6]
2961
0
Query!
Ethics committee country [6]
2961
0
Australia
Query!
Date submitted for ethics approval [6]
2961
0
Query!
Approval date [6]
2961
0
Query!
Ethics approval number [6]
2961
0
TMC-CAN-05-02
Query!
Summary
Brief summary
Each year over 1 million patients globally undergo diagnostic angiography and are discovered to have atherosclerotic plaque amenable to percutaneous coronary intervention (PCI). This area has been extensively researched and benefit shown with the use of aspirin, and more recently 300mg loading dose and 75mg maintenance dose of clopidogrel. Despite the apparent benefit, many patients still do not receive a loading dose (either deliberately – as there is a reasonable probability of being triaged to CABG) or because there is insufficient time (stable patients undergoing diagnostic angiogram who proceed immediately to PCI). Cangrelor is a new drug being developed, which in early phase trials appears to be safe and well tolerated & will provide platelet inhibition throughout the infusion with full recovery of platelet function within 60min of stopping the infusion. This trial aims to demonstrate the efficacy of cangrelor compared to clopidogrel in patients requiring PCI. The primary endpoints to be measured will be all cause mortality, myocardial infarction (MI) and ischemia driven reinfarction (IDR) at 48hrs and 1 month, then mortality at 1year. This study will employ double blind and double dummy tachniques in addition to an active control. Subjects, Investigators, Study Monitor, Data Analyst and the sponsor The Medicines Company will be blinded.
Query!
Trial website
Query!
Trial related presentations / publications
Query!
Public notes
Query!
Contacts
Principal investigator
Name
35146
0
Query!
Address
35146
0
Query!
Country
35146
0
Query!
Phone
35146
0
Query!
Fax
35146
0
Query!
Email
35146
0
Query!
Contact person for public queries
Name
10153
0
Ms Caroline Thomas
Query!
Address
10153
0
Cardiology Research
Flinders Medical Centre
1 Flinders Drive
Bedford Park SA 5042
Query!
Country
10153
0
Australia
Query!
Phone
10153
0
+61 8 82044440
Query!
Fax
10153
0
+61 8 82045000
Query!
Email
10153
0
[email protected]
Query!
Contact person for scientific queries
Name
1081
0
Associate Professor Derek Chew
Query!
Address
1081
0
Cardiac Services
Flinders Medical Centre
Bedford Park SA 5042
Query!
Country
1081
0
Australia
Query!
Phone
1081
0
+61 8 84042001
Query!
Fax
1081
0
+61 8 84042150
Query!
Email
1081
0
[email protected]
Query!
No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
Download to PDF