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Emergency Department (ED) Bedside UltraSound & Satisfaction Trial (BUSS Trial): A Randomised Controlled Trial of Bedside Echocardiogram in patients with ‘low risk’ chest pain in the ED.

Emergency Department (ED) Bedside UltraSound & Satisfaction Trial (BUSS Trial): A Randomised Controlled Trial of Bedside Echocardiogram in adult patients with ‘low risk’ chest pain in the ED.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12621000717853
Acronym
BUSS Trial
Enrollment
45
Registered
2021-06-09
Start date
2019-04-01
Completion date
2023-12-31
Last updated
2021-06-14

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 objective of the study is to assess at whether a bedside Echocardiogram (cardiac ultrasound) improves patient satisfaction of the emergency department performance. Adults with low risk chest pain will be recruited to intervention and control groups. The intervention group will receive a bedside echocardiogram and the outcome measure will be to assess patient satisfaction. An Echocardiogram is not routinely part of the chest pain assessment in ED. The hypothesis of the study is that participants with chest pain who receive an echocardiogram will have higher satisfaction scores compared to those who do not receive an echocardiogram.

Interventions

The primary outcome measure is a patient satisfaction survey regarding their treatment/stay in ED. Patients with low-risk chest pain will undergo standard assessment. This can include doctor’s assessment, blood tests including cardiac markers such as two troponin blood tests, xrays and CT scans. If the patient has been deemed as ‘low risk’ chest pain (i.e their troponin result is negative and/or other tests are negative) and are likely to be discharged, then they are usually admitted to ED Sho

The primary outcome measure is a patient satisfaction survey regarding their treatment/stay in ED. Patients with low-risk chest pain will undergo standard assessment. This can include doctor’s assessment, blood tests including cardiac markers such as two troponin blood tests, xrays and CT scans. If the patient has been deemed as ‘low risk’ chest pain (i.e their troponin result is negative and/or other tests are negative) and are likely to be discharged, then they are usually admitted to ED Short stay area while awaiting the repeat troponin blood test in 2 hour’s time. During the 2 hour period while patients are awaiting their repeat troponin eligible participants will be randomised to the intervention and control groups. The intervention group will undergo a single bedside cardiac ultrasound performed by an Emergency Physician trained in cardiac ultrasound or ED registrar with supervision by Emergency Physician. The ultrasound scan will be performed using Phillips Sparq Ultrasound Machine (Phased array probe) or similar point-of-care ultrasound device, and be performed using a documented protocol. Fidelity to the intervention will be monitored on review of each of the patient scans. Both intervention and control groups will complete a satisfaction/feedback surveys prior to final discharge .

Sponsors

Dr Vijay Manivel
Lead SponsorIndividual

Study design

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

Eligibility

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

Inclusion criteria

Inclusion criteria - Age greater than or equal to 18 years - History of chest pain on presentation to ED - Non-Trauma related chest pain - Low risk chest pain (no new ECG changes, negative troponins, Musculoskeletal chest pain, chest pain due to Upper GI pathology)

Exclusion criteria

Exclusion criteria - Age < 18 - Trauma related chest pain - Critically ill patients requiring urgent cardiac interventions - Unable to consent or provide satisfaction feedback (e.g due to language barrier, refusal to provide consent, intoxicated, cognitive impairment etc) - Patients who receive a formal cardiac ultrasound from cardiovascular and ICU labs

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026