Development and validation of a diagnostic alarm for monitoring anaesthesia related adverse events

Status

Not yet recruiting

Phases

Unknown

Study type

Observational

Source

ANZCTR

Registry ID

ACTRN12606000319572

Enrollment

Registered

2006-07-24

Start date

2006-09-01

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

The primary purpose of the protocol is to detect adverse events during anaesthesia using a computer and verify the diagnosis by the clinicians's assessment (in real time)

Interventions

Observation of hypovolaemia - for duration of operations

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

Patients having moderate to major surgery where blood loss is expected.

Exclusion criteria

Inability to give informed consent.

Outcome results