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The Australian Emergency Procedural Sedation Database; A multi-centre observational study of the practice of Procedural Sedation in Australian Emergency Departments (ED)

Prospective, multicentre, observational study of all patients undergoing Procedural Sedation in the Emergency Department to evaluate current practices, future trends and safety outcomes.

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ANZCTR
Registry ID
ACTRN12621000198820
Enrollment
1000
Registered
2021-02-25
Start date
2021-04-01
Completion date
Unknown
Last updated
2021-03-01

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

Conditions

None listed

Brief summary

Procedural sedation to facilitate painful and non-painful procedures is a core skill of specialist emergency physicians (EPs) in Australasia. Our goal is to establish a national procedural sedation dataset to monitor practice for trends in techniques and safety on a large scale over time. This will collect data on current practices around procedural sedation, including patient selection and optimisation, staffing, medication use, monitoring modalities and rates of procedural success and sedation complications. We hope that this database will form fertile ground for the exploration of future research hypotheses.

Interventions

We will record the indication for procedural sedation, the type of staff present and their roles, patient predicted markers of complexity, techniques (including medications, doses, monitoring and pre-oxygenation) and the occurrence of any complications prior to discharge from the emergency department. The study requires no active participation from patients, instead capturing data on current clinical practice via direct entry by clinicians into an electronic database. We aim to collect data for

We will record the indication for procedural sedation, the type of staff present and their roles, patient predicted markers of complexity, techniques (including medications, doses, monitoring and pre-oxygenation) and the occurrence of any complications prior to discharge from the emergency department. The study requires no active participation from patients, instead capturing data on current clinical practice via direct entry by clinicians into an electronic database. We aim to collect data for one year for initial evaluation with the goal of continuing on an ongoing basis.

Sponsors

Ashley Loughman
Lead SponsorIndividual

Eligibility

Sex/Gender
All
Healthy volunteers
No

Inclusion criteria

All patients undergoing procedural sedation within Australian Emergency Departments on an ongoing basis

Exclusion criteria

No specific exclusion criteria

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026