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
Trial registered on ANZCTR


Registration number
ACTRN12619000960156
Ethics application status
Approved
Date submitted
21/06/2019
Date registered
8/07/2019
Date last updated
17/11/2020
Date data sharing statement initially provided
8/07/2019
Type of registration
Prospectively registered

Titles & IDs
Public title
Assessment of a New Novel Fluid Monitoring Device in Heart Failure Patients
Scientific title
Assessment of a New Novel Fluid Monitoring Device in Heart Failure Patients
Secondary ID [1] 298571 0
CT-2019-CTN-01580-1
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Congestive heart failure (CHF) 313410 0
Condition category
Condition code
Cardiovascular 311844 311844 0 0
Other cardiovascular diseases

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Patients who provide consent to take part in the study will be asked to wear an adhesive leg band strip with 5 bio-impedance sensors attached horizontally around the back of their calf. This leg band will remain attached for up to 8 hours at a time and data will be collected over a 3 day period. The leg band will be connected to a data recording unit which can be disconnected when required.
Intervention code [1] 314831 0
Diagnosis / Prognosis
Comparator / control treatment
No control group
Control group
Uncontrolled

Outcomes
Primary outcome [1] 320516 0
The primary objective of the study is to record changes in bio-impedance over a three day period in hospitalised heart failure patients.
Timepoint [1] 320516 0
Participants will be directly recruited for the study following admission to the heart failure clinic or from the cardiac ward. Patients will be recruited when showing signs of significant fluid overload associated with a heart failure condition.
Secondary outcome [1] 371884 0
N/A
Timepoint [1] 371884 0
N/A

Eligibility
Key inclusion criteria
• Male and female Age 18 years+
• Heart failure Condition
• Hospitalised with significant fluid overload for fluid offload.
• Ability to give written informed consent and agree to adhere to all protocol requirements.
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
• Patient has been prescribed to wear TED stockings throughout the duration of their hospital stay.
• Leg prosthesis or other disorders making measurement of leg oedema difficult or inadvisable.
• Pregnancy

Study design
Purpose of the study
Diagnosis
Allocation to intervention
Non-randomised trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Open (masking not used)
Who is / are masked / blinded?



Intervention assignment
Single group
Other design features
Phase
Not Applicable
Type of endpoint/s
Efficacy
Statistical methods / analysis
This study will utilise 20 participants in total.

The data collected from this study will be analysed to determine whether a correlation can be seen between bio-impedance readings and changes in fluid status in heart failure patients.

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
12/08/2019
Actual
21/08/2019
Date of last participant enrolment
Anticipated
6/01/2020
Actual
21/01/2020
Date of last data collection
Anticipated
17/01/2020
Actual
24/01/2020
Sample size
Target
20
Accrual to date
Final
20
Recruitment in Australia
Recruitment state(s)
VIC
Recruitment outside Australia
Country [1] 21631 0
Singapore
State/province [1] 21631 0
Singapore

Funding & Sponsors
Funding source category [1] 303109 0
Commercial sector/Industry
Name [1] 303109 0
Safehouse Innovation Ltd
Country [1] 303109 0
Australia
Primary sponsor type
Commercial sector/Industry
Name
Safehouse Innovation Ltd
Address
Level 4
543 Bridge Road (PO Box 12)
Richmond
Victoria
Australia
3121
Country
Australia
Secondary sponsor category [1] 303103 0
None
Name [1] 303103 0
Address [1] 303103 0
Country [1] 303103 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 303659 0
Alfred Health Ethics Committee
Ethics committee address [1] 303659 0
Ethics committee country [1] 303659 0
Australia
Date submitted for ethics approval [1] 303659 0
06/06/2019
Approval date [1] 303659 0
05/08/2019
Ethics approval number [1] 303659 0

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

Contacts
Principal investigator
Name 94414 0
Prof David Kaye
Address 94414 0
Alfred Health
55 Commercial Rd,
Melbourne
VIC
3004
Country 94414 0
Australia
Phone 94414 0
+61 390762000
Fax 94414 0
Email 94414 0
[email protected]
Contact person for public queries
Name 94415 0
Kevin Noble
Address 94415 0
Grey Innovation Pty Ltd
Level 4
543 Bridge Road (PO Box 12)
Richmond
Victoria
Australia
3121
Country 94415 0
Australia
Phone 94415 0
+61 3 8459 6999
Fax 94415 0
Email 94415 0
[email protected]
Contact person for scientific queries
Name 94416 0
Kevin Noble
Address 94416 0
Grey Innovation Pty Ltd
Level 4
543 Bridge Road (PO Box 12)
Richmond
Victoria
Australia
3121
Country 94416 0
Australia
Phone 94416 0
+61 3 8459 6999
Fax 94416 0
Email 94416 0
[email protected]

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
No/undecided IPD sharing reason/comment
Data to inform subsequent product development only


What supporting documents are/will be available?

Doc. No.TypeCitationLinkEmailOther DetailsAttachment
2419Study protocol  [email protected]



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.