RecruitingPhase 4ACTRN12611000385943
Effect of Propofol on Ability to Drive
Estimation of the simulated driving ability of post-surgical patients with varying Propofol plasma concentrations
Sponsor
Monash Medical Centre
Enrollment
20 participants
Start Date
Jun 14, 2011
Study Type
Interventional
Conditions
Eligibility
Sex: Both males and femalesMin Age: 18 Yearss
Inclusion Criteria2
- Patients undergoing day-case surgery at Monash Medical Centre;
- Patients that are expected to be receiving a Propofol based anaesthetic.
Exclusion Criteria9
- Below 18 years of age;
- Insufficient English comprehension to understand consent form;
- Too ill to participate as judged by the Prinipal Investigator;
- Patient refusal;
- Known allergy to Propofol;
- Absent limb or limbs;
- Documented cerebrovascular accident;
- Documented intra-cranial space occupying lesion;
- No current driver’s licence.
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Interventions
Administration of Propofol via intravenous infusion
a) The dose will be titrated to achieve an estimated plasma concentration of 0.5, 1.0, 1.5, 2.0, 2.5, 3.0 mg/mL in stepwise progression
b) the inf
Administration of Propofol via intravenous infusion a) The dose will be titrated to achieve an estimated plasma concentration of 0.5, 1.0, 1.5, 2.0, 2.5, 3.0 mg/mL in stepwise progression b) the infusion will be continuous and will not exceed 30 minutes
Locations(1)
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ACTRN12611000385943