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Trial registered on ANZCTR


Registration number
ACTRN12607000004460
Ethics application status
Approved
Date submitted
7/12/2006
Date registered
4/01/2007
Date last updated
22/02/2008
Type of registration
Prospectively registered

Titles & IDs
Public title
The effect of remote ischaemic preconditioning on lowering postoperative myocardial troponin I release in children with congenital heart disease undergoing cardiopulmonary bypass.
Scientific title
The effect of remote ischaemic preconditioning on lowering postoperative myocardial troponin I release in children with congenital heart disease undergoing cardiopulmonary bypass.
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Congenital heart disease witithin neonates 1507 0
Condition category
Condition code
Cardiovascular 1605 1605 0 0
Other cardiovascular diseases

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Preconditioning as a method of myocardial protection at the time of repair of congenital heart disease. Patients will be randomised to control or remote ischaemic preconditioning. The remote ischaemic preconditioning protocol will be by 4 cycles of 5 minutes of lower limb ischaemia induced by inflating a blood pressure cuff to 15 mmHg greater than systolic blood pressure placed around the thigh, followed by 5 minutes of reperfusion.
Intervention code [1] 1490 0
Prevention
Comparator / control treatment
Controls will have the blood pressure cuff placed loosely around the thigh but not inflated. The total time for the preconditioning protocol and the sham is therefore 40 minutes.
Control group
Placebo

Outcomes
Primary outcome [1] 2214 0
Postoperative levels of troponin I will be measured from blood samples
Timepoint [1] 2214 0
Blood samples taken immediately preoperatively and then at 3, 6 and 24 hours postoperatively.
Secondary outcome [1] 3858 0
Cardiac output, lung function, systemic inflammatory response.
Timepoint [1] 3858 0
Each of these will be assessed at 3, 6 and 24 hours postoperatively.
Secondary outcome [2] 3859 0
Inflammatory response in the form of blood levels of TNF-alpha.
Timepoint [2] 3859 0
Assessed immediately preoperatively.

Eligibility
Key inclusion criteria
Neonates undergoing open heart surgery for repair of congenital defects will be recruited. Specifically, children undergoing the arterial switch procedure and the Norwood procedure will be studied.
Minimum age
1 Days
Maximum age
28 Days
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
Patients with chromosomal defects, associated congenital lung malformations, and haematological disorders and those older than 28 days will be excluded.

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Sealed opaque envelopes
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Randomisation will be by block and stratified by the two diagnostic groups (Norwood and Transposition).
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?



Intervention assignment
Parallel
Other design features
Subjects, laboratory staff analying blood samples, bedside medical staff will all be blinded.
Phase
Phase 1
Type of endpoint/s
Efficacy
Statistical methods / analysis

Recruitment
Recruitment status
Recruiting
Date of first participant enrolment
Anticipated
Actual
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)

Funding & Sponsors
Funding source category [1] 1749 0
Government body
Name [1] 1749 0
National Heart Foundation
Country [1] 1749 0
Australia
Funding source category [2] 3087 0
Charities/Societies/Foundations
Name [2] 3087 0
Heartkids and Manchester Unity
Country [2] 3087 0
Australia
Primary sponsor type
Individual
Name
Michael Cheung
Address
Royal Childrens Hospital, Parkville, Victoria 3052
Country
Australia
Secondary sponsor category [1] 1546 0
Individual
Name [1] 1546 0
Lara Shekerdemian
Address [1] 1546 0
Royal Childrens Hospital, Parkville, VIC 3052
Country [1] 1546 0
Australia
Secondary sponsor category [2] 1547 0
Individual
Name [2] 1547 0
Ian Mackenzie
Address [2] 1547 0
Royal Childrens Hospital, Parkville, VIC 3052
Country [2] 1547 0
Australia
Secondary sponsor category [3] 1548 0
Individual
Name [3] 1548 0
Yves D'Udekem
Address [3] 1548 0
Royal Childrens Hospital, Parkville, VIC 3052
Country [3] 1548 0
Australia
Secondary sponsor category [4] 1549 0
Individual
Name [4] 1549 0
Steve Horten
Address [4] 1549 0
Royal Childrens Hospital, Parkville, VIC 3052
Country [4] 1549 0
Australia
Secondary sponsor category [5] 1550 0
Individual
Name [5] 1550 0
Polly Hardy
Address [5] 1550 0
Royal Childrens Hospital, Parkville, VIC 3052
Country [5] 1550 0
Australia

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 3246 0
Ethics and Human Research Committee of the Royal Childrens Hospital Melbourne
Ethics committee address [1] 3246 0
Ethics committee country [1] 3246 0
Australia
Date submitted for ethics approval [1] 3246 0
01/05/2006
Approval date [1] 3246 0
14/03/2007
Ethics approval number [1] 3246 0
26091A

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 27424 0
Address 27424 0
Country 27424 0
Phone 27424 0
Fax 27424 0
Email 27424 0
Contact person for public queries
Name 10679 0
Michael Cheung
Address 10679 0
Department of Cardiology
Royal Children's Hospital
Parkville VIC 3052
Country 10679 0
Australia
Phone 10679 0
+61 3 93455718
Fax 10679 0
Email 10679 0
Contact person for scientific queries
Name 1607 0
Michael Cheung
Address 1607 0
Department of Cardiology
Royal Children's Hospital
Parkville VIC 3052
Country 1607 0
Australia
Phone 1607 0
+61 3 93455718
Fax 1607 0
Email 1607 0

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.