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Comparison of a single dose of intravenous paracetamol with rectal paracetamol and placebo in the treatment of mild to moderate postoperative pain

Comparison of a single dose of intravenous paracetamol with rectal paracetamol and placebo in the treatment of mild to moderate postoperative pain

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12605000786695
Enrollment
45
Registered
2005-12-12
Start date
2006-01-16
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

Single dose of either intravenous or rectal paracetamol prior to induction of anaesthesia

Sponsors

Bristol-Myers Squibb
Lead SponsorCommercial sector/Industry

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

Source: ANZCTR · Data processed: Feb 4, 2026