Comparative effect of intraoperative propacetamol administration versus placebo on morphine consumption after elective reduction mammoplasty

Completed

• Conditions: Morphine consumption and postoperative pain after intraoperative administration of placebo or propacetamol; Surgery; Pain, not elsewhere classified

• Registration Number: ISRCTN71723173
• Lead Sponsor: Fight Against Pain Committee (Comité de Lutte contre la Douleur [CLUD]) (France)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2004-08-27
• Last Update Posted: 13 January 2015

Recruitment & Eligibility

• Status: Completed
• Sex: Female
• Target Recruitment: 36

Inclusion Criteria

1. Informed consent adult women above 18 years
2. American Society of Anesthesiologists (ASA) I and II

Exclusion Criteria

1. Preoperative use of analgesic drugs
2. Body mass index = 35
3. American Society of Anesthesiology physical status = 3
4. Sensitivity to paracetamol

Study & Design

• Study Type: Interventional
• Study Design: Not specified