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Trial registered on ANZCTR
Registration number
ACTRN12621000164897
Ethics application status
Approved
Date submitted
19/01/2021
Date registered
17/02/2021
Date last updated
17/02/2021
Date data sharing statement initially provided
17/02/2021
Type of registration
Prospectively registered
Titles & IDs
Public title
Does preoperative muscle mass predict outcomes after heart and/or lung transplantation
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Scientific title
Preoperative assessment of muscle mass and heart rate variability as predictors of outcome in patients undergoing heart and/or lung transplantation
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Secondary ID [1]
303207
0
None
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Heart transplantation
320347
0
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Lung transplantation
320348
0
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Sarcopenia
320349
0
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Condition category
Condition code
Surgery
318260
318260
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0
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Other surgery
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Musculoskeletal
318609
318609
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0
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Other muscular and skeletal disorders
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Intervention/exposure
Study type
Observational
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Patient registry
False
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
The rectus femoris muscle will be measured using ultrasound. This will occur in the outpatient clinic prior to surgery. The ultrasound takes less than 5 minutes and will be performed by an anaesthetist who is part of the research team. A 5 minute electrocardiograph (ECG) recording will also be performed for subsequent analysis
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Intervention code [1]
319515
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Early Detection / Screening
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Comparator / control treatment
No control group
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
326243
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Hospital Length of Stay - assessed using the hospital electronic medical record
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Assessment method [1]
326243
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Timepoint [1]
326243
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Discharge from hospital
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Secondary outcome [1]
390705
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Length of Stay in ICU - assessed using the hospital electronic medical record
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Assessment method [1]
390705
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Timepoint [1]
390705
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Discharge from ICU
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Secondary outcome [2]
390706
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In-hospital Mortality - assessed using the hospital electronic medical record
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Assessment method [2]
390706
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Timepoint [2]
390706
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Date of death in hospital
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Eligibility
Key inclusion criteria
All patients undergoing heart and/or lung transplantation
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
None
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Study design
Purpose
Screening
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Duration
Cross-sectional
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Selection
Defined population
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Timing
Prospective
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Statistical methods / analysis
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
1/05/2021
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Actual
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Date of last participant enrolment
Anticipated
30/04/2023
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Actual
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Date of last data collection
Anticipated
30/05/2023
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Actual
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Sample size
Target
100
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
NSW
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Funding & Sponsors
Funding source category [1]
307611
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Hospital
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Name [1]
307611
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Department of Anaesthesia, St Vincent’s Hospital
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Address [1]
307611
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Level 4
St Vincent’s Hospital
390 Victoria St,
Darlinghurst,
NSW 2010
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Country [1]
307611
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Australia
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Primary sponsor type
Hospital
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Name
St Vincent’s Hospital
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Address
390 Victoria St,
Darlinghurst,
NSW 2010
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Country
Australia
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Secondary sponsor category [1]
308302
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None
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Name [1]
308302
0
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Address [1]
308302
0
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Country [1]
308302
0
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
307663
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St Vincent’s Hospital Human Research & Ethics Committee
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Ethics committee address [1]
307663
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St Vincent’s Hospital 390 Victoria St Darlinghurst NSW 2010
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Ethics committee country [1]
307663
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Australia
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Date submitted for ethics approval [1]
307663
0
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Approval date [1]
307663
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21/12/2020
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Ethics approval number [1]
307663
0
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Summary
Brief summary
Heart and/or lung transplantation is performed in patients with significant co-morbidities and burden of disease. Their peri-operative period is high risk and recovery may be prolonged due to the risk of complications. There is considerable effort applied to appropriate risk stratification and selection of these patients prior to listing for transplantation. Recently sarcopenia has been used as a surrogate for frailty. Patients undergoing heart and/or lung transplant surgery may be particularly susceptible to the risks associated with frailty. In heart/lung transplant surgical patients objective measurements of sarcopenia has been difficult and not fully investigated. The hypothesis of this study is that reduced cross sectional area of the rectus femoris muscles as assessed by ultrasound and/or reduced heart rate variability will be associated with poorer outcomes amongst cardio-thoracic patients undergoing major surgery.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
108050
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Dr Catherine Ashes
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Address
108050
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Department of Anaesthesia
St Vincent’s Hospital
390 Victoria Road
Darlinghurst
NSW 2010
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Country
108050
0
Australia
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Phone
108050
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+61 2 83823200
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Fax
108050
0
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Email
108050
0
[email protected]
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Contact person for public queries
Name
108051
0
Catherine Ashes
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Address
108051
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Department of Anaesthesia
St Vincent’s Hospital
390 Victoria Road
Darlinghurst
NSW 2010
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Country
108051
0
Australia
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Phone
108051
0
+61 2 83823200
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Fax
108051
0
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Email
108051
0
[email protected]
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Contact person for scientific queries
Name
108052
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Catherine Ashes
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Address
108052
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Department of Anaesthesia
St Vincent’s Hospital
390 Victoria Road
Darlinghurst
NSW 2010
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Country
108052
0
Australia
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Phone
108052
0
+61 2 83823200
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Fax
108052
0
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Email
108052
0
[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
No individual participant data will be shared due to the risk of patients undergoing rare surgery subsequently being able to be indentified. ie heart transplant recipients. Even though the data will be de-identified, demographic and background health data will potentially allow individual identification of patients. Ie heart transplantation is uncommon and knowing the age and gender of a patient who received a heart transplant in any given year may allow identification of that patient. Only pooled data de-identified data will be released via publication as approved by our research and ethics committee
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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