A randomised double-blind comparative trial investigating the level of pain experienced on induction of anaesthesia using either standard Propofol 1% or Propofol-Lipuro 1% with or without the addition of lignocaine 2% (1:10 ratio)
Completed
- Conditions
- Surgery: AnaesthesiaSurgeryAnaesthesia
- Registration Number
- ISRCTN10285854
- Lead Sponsor
- Record Provided by the NHSTCT Register - 2004 Update - Department of Health (UK)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients undergoing uncomplicated elective surgery
Exclusion Criteria
Not provided at time of registration
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method