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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT02012179




Registration number
NCT02012179
Ethics application status
Date submitted
10/12/2013
Date registered
16/12/2013

Titles & IDs
Public title
SODIUM-HF: Study of Dietary Intervention Under 100 MMOL in Heart Failure
Scientific title
The Long Term Effects of Dietary Sodium Restriction on Clinical Outcomes in Patients With Heart Failure
Secondary ID [1] 0 0
MOP130275
Universal Trial Number (UTN)
Trial acronym
SODIUM-HF
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Heart Failure 0 0
Condition category
Condition code
Cardiovascular 0 0 0 0
Coronary heart disease
Cardiovascular 0 0 0 0
Other cardiovascular diseases

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Other interventions - Low sodium diet

Experimental: Low sodium diet - Low sodium diet (65 mmol or 1500 mg/day)

No intervention: Usual Care - General advice to limit dietary sodium as it is provided during routine clinic practice


Other interventions: Low sodium diet
Low sodium diet (65 mmol or 1500 mg/day)
Intervention code [1] 0 0
Other interventions
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Composite Clinical Outcomes
Timepoint [1] 0 0
12 months
Secondary outcome [1] 0 0
Exercise capacity
Timepoint [1] 0 0
12 months
Secondary outcome [2] 0 0
NYHA functional class
Timepoint [2] 0 0
12 months
Secondary outcome [3] 0 0
Quality of life (KCCQ)
Timepoint [3] 0 0
12 months

Eligibility
Key inclusion criteria
* Patients recruited if they are 18+ years or older, with confirmed diagnosis of HF (both reduced and preserved systolic function are eligible), NYHA class II-III, and willing to sign informed consent.
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
Subjects will be excluded if:

* Average dietary intake of <1500 mg/ day by a quantitative or semi-quantitative method
* Serum sodium <130mmol/L
* Renal failure (glomerular filtration rate <30 mL/min)
* Hepatic failure
* Uncontrolled thyroid disorder
* Cardiac device (ICD or CRT) or revascularization procedure (PCI or CABG) in previous month or planned in next 3 months
* Hospitalization due to cardiovascular causes in previous 1 month
* Uncontrolled atrial fibrillation (resting heart rate >90 bpm)
* Active malignancy
* Moderate-severe dementia
* Enrolled in another interventional research study
* Patients will be excluded, if in the opinion of the investigator, another condition exists that would preclude dietary compliance or compliance with the protocol.

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)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?


The people assessing the outcomes
Intervention assignment
Parallel
Other design features
Phase
Phase 3
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
24/03/2014
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
1/01/2023
Sample size
Target
Accrual to date
Final
806
Recruitment in Australia
Recruitment state(s)
Recruitment hospital [1] 0 0
The Prince Charles Hospital - Chermside
Recruitment hospital [2] 0 0
St. Vincent's Hospital Sydney - Darlinghurst
Recruitment hospital [3] 0 0
Metro North Hospital and Health Service - Herston
Recruitment postcode(s) [1] 0 0
- Chermside
Recruitment postcode(s) [2] 0 0
- Darlinghurst
Recruitment postcode(s) [3] 0 0
- Herston
Recruitment outside Australia
Country [1] 0 0
Canada
State/province [1] 0 0
Alberta
Country [2] 0 0
Canada
State/province [2] 0 0
British Columbia
Country [3] 0 0
Canada
State/province [3] 0 0
Manitoba
Country [4] 0 0
Canada
State/province [4] 0 0
Nova Scotia
Country [5] 0 0
Canada
State/province [5] 0 0
Ontario
Country [6] 0 0
Canada
State/province [6] 0 0
Saskatchewan
Country [7] 0 0
Chile
State/province [7] 0 0
Osorno
Country [8] 0 0
Chile
State/province [8] 0 0
Temuco
Country [9] 0 0
Mexico
State/province [9] 0 0
Mexico City
Country [10] 0 0
New Zealand
State/province [10] 0 0
Auckland
Country [11] 0 0
New Zealand
State/province [11] 0 0
Christchurch

Funding & Sponsors
Primary sponsor type
Other
Name
University of Alberta
Address
Country

Ethics approval
Ethics application status

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

Contacts
Principal investigator
Name 0 0
Justin Ezekowitz, MBBCh
Address 0 0
University of Alberta
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
No/undecided IPD sharing reason/comment


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

No documents have been uploaded by study researchers.


Results not provided in https://clinicaltrials.gov/study/NCT02012179