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Pre-Hospital Lung Ultrasound in Infants Presenting with Respiratory Illness: A Feasibility Study

Pre-Hospital Lung Ultrasound in Infants Presenting with Respiratory Illness: A Feasibility Study

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12617000962336
Enrollment
100
Registered
2017-07-05
Start date
2017-08-01
Completion date
Unknown
Last updated
2017-07-10

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

Conditions

None listed

Brief summary

Respiratory illness is a common presentation among the paediatric population and many will have multiple presentations during their lifetime. Bronchiolitis is one of the common viral-induced lower respiratory tract infections (LRTI), particularly during Winter, and can often result in hospital admission. This project proposes to demonstrate the use of pre-hospital point-of-care lung ultrasound is practical in the diagnosis of bronchiolitis and the ultrasound images can be reliably interpreted by Retrieval Doctors.

Interventions

Pre-hospital point-of-care ultrasound of the lungs will be performed by Central Australian Retrieval Doctors at the clinic/remote health centre/site of retrieval prior to transport to Alice Springs Hospital. The participants will have warmed ultrasound gel applied to four areas on the chest (2 right and 2 left) and bedside ultrasound scanning carried-out. The de-identified images will then be saved and the performing medical officer will record their findings on the study proforma. The interve

Pre-hospital point-of-care ultrasound of the lungs will be performed by Central Australian Retrieval Doctors at the clinic/remote health centre/site of retrieval prior to transport to Alice Springs Hospital. The participants will have warmed ultrasound gel applied to four areas on the chest (2 right and 2 left) and bedside ultrasound scanning carried-out. The de-identified images will then be saved and the performing medical officer will record their findings on the study proforma. The intervention fidelity and any difficulties encountered will be recorded by the performing doctor on the study proforma. If inadequate images are obtained, this will be recorded as such.

Sponsors

Central Australian Health Network
Lead SponsorGovernment body

Study design

Allocation
Non-randomised trial
Primary purpose
Diagnosis

Eligibility

Sex/Gender
All
Age
No minimum to 18 Months
Healthy volunteers
No

Inclusion criteria

Children <18 months of age with symptoms consistent with a respiratory illness, including shortness of breath, increased work of breathing, coryza, fever and/or cough requiring retrieval via the Central Australian Retrieval Service for management in hospital

Exclusion criteria

Age > 2 years (as per diagnostic criteria for Bronchiolitis) No symptoms of respiratory illness Refusal of guardian/parents to assent to study participation

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026