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Pre-Hospital Assessment of Noninvasive Tissue Oximetry Monitoring

CareFlight Prospective Observational Trial of Noninvasive Cerebral Oximetry in Pre-Hospital Trauma Patients to Assess Long Term Functional Outcomes

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ANZCTR
Registry ID
ACTRN12611001124921
Acronym
The PHANTOM Study
Enrollment
1210
Registered
2011-10-27
Start date
2014-07-06
Completion date
Unknown
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

A lot of the things we do when looking after patients with significant injuries after accidents relies on using monitors to provide us with information. When it comes to the brain, we often measures things elsewhere in the body and assume that if those things are normal, we're doing the best we can for the brain, but we can't be sure. This study is designed to look at a kind of monitor that you can apply to the skin which gives you information directly about oxygen balance in the brain. The hypothesis is that there is an association between the values shown by the monitor in injured patients and how well they recover after their injury - meaning that if the numbers are abnormal, it correlates with worse recovery later.

Interventions

Observation of cerebral oximetry parameters during pre-hospital care of patients suffering traumatic injury patient management and transport to hospital. The duration of observation will vary depending on the nature of the pre-hospital accident, treatment time and distance for transport to hospital. Historical experience indicates the average time elapsed from the time of arrival of the treating team until the patient is in hospital is approximately 40 minutes.

Sponsors

Dr Andrew Weatherall
Lead SponsorIndividual

Eligibility

Sex/Gender
All
Age
1 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

All patients being transported by a rapid response trauma response team (incorporating a doctor-paramedic team). This may include, but would not be limited to: Patients with a blunt force mechanism for head injury with initial evidence of reduced level of consciousness. Patients with major blunt mechanism thoracic and abdominal trauma. Patients with major haemorrhage. Patients with penetrating trauma. Patients with severe burn injuries. Patients with major extremity injury. Patients with trauma and major compression injury.

Exclusion criteria

Patients less than 1 year old or more than 70 years old. Patients with a history of previous neurological disease or neurological trauma. Patients with no mechanism for trauma. Patients with significant haematomas or lacerations in the forehead area. Patients in whom consent is not obtained at a later time

Outcome results

None listed

Source: ANZCTR · Data processed: Mar 19, 2026