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

Recruiting

• Conditions: Postoperative pain; Other - Pain management

• Registration Number: ACTRN12605000786695
• Lead Sponsor: Bristol-Myers Squibb

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2005-12-12
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 45

Inclusion Criteria

Female patients undergoing minor laparoscopic gynaecological surgeryASA I and II.

Exclusion Criteria

Allergy to paracetamol and/or morphineHepatic or renal dysfunction.

Study & Design

• Study Type: Interventional
• Study Design: Not specified