None listed
Conditions
Interventions
Single dose of either intravenous or rectal paracetamol prior to induction of anaesthesia
Sponsors
Bristol-Myers Squibb
Study design
Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used)
Eligibility
Sex/Gender
All
Age
0 to No maximum
Healthy volunteers
No
Inclusion criteria
Female patients undergoing minor laparoscopic gynaecological surgeryASA I and II.
Exclusion criteria
Allergy to paracetamol and/or morphineHepatic or renal dysfunction.
Outcome results
None listed