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Propofol or Ketofol for Emergency Medicine Procedural Sedation- A Randomised Controlled Trial utilising eHealth methodology.

"Ketafol v Propofol in Emergency Department Procedural Sedation to reduce adverse events".

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12610001056088
Acronym
POKEM Study
Enrollment
350
Registered
2010-12-01
Start date
2011-02-01
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

Interventions

This study will compare the use of a commonly used sedative drug – propofol, used alone or in combination with another drug that has sedative and pain relieving properties called ketamine. The idea is that using a combination of the two drugs together will result in lower doses of each being used if they were to be used independent of one another. 1) Initial Dose in ml equates to 0.5mg kg Propofol alone or 0.25mg/kg Ketamine and propofol in combination 2) Subsequent doses are at half those amoun

This study will compare the use of a commonly used sedative drug – propofol, used alone or in combination with another drug that has sedative and pain relieving properties called ketamine. The idea is that using a combination of the two drugs together will result in lower doses of each being used if they were to be used independent of one another. 1) Initial Dose in ml equates to 0.5mg kg Propofol alone or 0.25mg/kg Ketamine and propofol in combination 2) Subsequent doses are at half those amounts minutely prn 3) The mode of administration is Intravenous injection.

Sponsors

QE II Hospital
Lead SponsorHospital

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

Need for emergency department procedural sedation

Exclusion criteria

Inability to provide consent, age <18yrs, pregnancy, soy or egg allergy, Glasgow Coma Scale<15, hypotension, severe systemic disease (American Society Anesthesiologists class IV or greater), uncontrolled hypertension (Blood Pressure>160/90), patients with known Abdominal Aortic Aneurysm or symptomatic Ischaemic Heart Disease.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026