NCT01211158.

Trial name or title	Randomized double‐blind trial to evaluate ketamine‐propofol combination vs propofol alone for procedural sedation and analgesia in the emergency department
Methods	RCT, parallel design
Participants	Aged ≥14 years Deemed to require emergency department procedural sedation by attending physician
Interventions	Propofol (10 mg/mL) Ketofol (5 mg/mL propofol + 5 mg/mL ketamine)
Outcomes	Respiratory adverse events Oxygen desaturation, central apnoea, partial upper airway obstruction, complete upper airway obstruction, laryngospasm, clinically apparent pulmonary aspiration
Starting date	September 28, 2010
Contact information	G Andolfatto, Lions Gate Hospital, University of British Columbia Department of Emergency Medicine
Notes	clinicaltrials.gov register number: NCT01211158

RCT = randomized controlled trial.