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TAsmanian Study of Echocardiographic detection of Left ventricular dysfunction (TAS-ELF)

Study of heart failure outcomes in stage A heart failure patients screened using advanced echocardiography techniques.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12614000080628
Acronym
TAS-ELF
Enrollment
800
Registered
2014-01-22
Start date
2013-09-30
Completion date
2015-06-30
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

The aim of this project is to reduce the deaths caused by Heart Failure in Tasmania. This will be achieved through implementation of a screening program for cardiac dysfunction and the use of protective therapy that will limit the development of heart failure. We plan to show the benefit of testing by recruitment of "at risk" subjects from the community and randomising them to a screening program based on echocardiography. Patients with abnormalities will be entered into a program of cardio-protective therapy, supervised by their general practitioner. Endpoints: 6-minute walk at a minimum of 24 months and comparison of the rate of heart failure among groups.

Interventions

Inclusion of myocardial mechanics in screening echocardiography for heart failure. This screening test is envisaged at one point in time and the acquisition takes ~30 minutes.

Sponsors

Menzies Research Institute Tasmania
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Diagnosis
Masking
Blinded (masking used) (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Aged >65 years with one or more of the following; - diabetes (T2DM) - obesity - high blood pressure - past cancer chemotherapy - F/H of heart failure - known cardiac disease (but not existing heart failure)

Exclusion criteria

- Unable to provide written informed consent to participate in this study - Participating in another clinical research trial where randomized treatment would be unacceptable - History of >moderate valvular heart disease - History of previous heart failure - Existing medical therapy with beta blockers and ACE inhibitors - Contraindications/Intolerance to beta blockers or ACE inhibitors - Systolic BP <110mmHg - Pulse <60/minute - Baseline NYHA >2 - Oncologic life expectancy < 12 months - Inability to acquire interpretable images (identified from baseline echo)

Outcome results

None listed

Source: ANZCTR · Data processed: Mar 10, 2026