Type of Study:

Interventional

Study Design:

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Outcome Measure:

Visual analog scale (VAS) rating of pain

Outcome Time Frame:

0-24h after surgeries

Safety Issue:

Yes

Principal Investigator

XiaoFeng Shen, MD

Investigator Role:

Study Chair

Investigator Affiliation:

Nanjing Medical University

Authority:

China: Ministry of Health

Study ID:

NMU-2579-4FW

NCT ID:

NCT00519246

Start Date:

February 2007

Completion Date:

December 2007

Related Keywords:

• Pain, Postoperative
• Mastectomy
• Breast Neoplasms
• Non-Steroidal Anti-Inflammatory Agents
• Analgesia
• Pain, Postoperative