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Point-of-care ultrasound in patients with shortness of breath.

Point-of-Care Ultrasound (POCUS): Reducing Hospital Length of Stay in Patients with Dyspnoea

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12626000270314
Acronym
DysPOCUS trial
Enrollment
2
Registered
2026-03-04
Start date
2026-05-12
Completion date
2028-05-04
Last updated
2026-06-15

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

Conditions

None listed

Brief summary

A multicentre, randomised parallel group, open superiority trial. 900 patients 65 years old or older admitted to the general medicine ward with a primary presentation of dyspnoea will be allocated in a 1:1 ratio to receive a) usual care or b) usual care and POCUS of the heart, lungs and proximal lower limb veins, performed within 24 hours of ward admission. The main outcome assessed in length of hospital stay. Secondary outcomes include dyspnoea improvement, mortality and major adverse cardiovascular (MACE) measure at day 30 and 1 year

Interventions

Point of care ultrasound of the heart, lungs, and proximal lower limb veins will be performed once by a physician within the first 24 hours of hospital admission. The examination takes approximately 15 minutes on average and involves the use of a portable ultrasound machine with acoustic gel. The ultrasound transducer is placed over the patient’s chest, posterior thorax, and proximal lower limbs to obtain the required views. A structured report of the examination will be collected to assess adhe

Point of care ultrasound of the heart, lungs, and proximal lower limb veins will be performed once by a physician within the first 24 hours of hospital admission. The examination takes approximately 15 minutes on average and involves the use of a portable ultrasound machine with acoustic gel. The ultrasound transducer is placed over the patient’s chest, posterior thorax, and proximal lower limbs to obtain the required views. A structured report of the examination will be collected to assess adherence to the intervention protocol.

Sponsors

Melbourne health
Lead SponsorGovernment body

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

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

Inclusion criteria

Adults aged 65 years or older who are admitted to the internal medicine ward where the primary symptom leading to admission is dyspnoea regardless of the initial medical diagnosis (e.g decompensated heart failure, pneumonia, asthma)

Exclusion criteria

Exclusion criteria include having a computed tomography chest or CT pulmonary angiogram, point of care ultrasound performed by emergency physicians, being admitted to the ward more than 24 hours ago, or where death is expected within 48-hour.

Outcome results

None listed

Source: ANZCTR · Data processed: Jun 21, 2026