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Clinical Trial Summary

We conducted a prospective, randomized double-blind study to compare the effectiveness of intravenous paracetamol and dipyrone for preventing pain during early postoperative period in school-age children undergoing lower abdominal surgery with spinal anesthesia.


Clinical Trial Description

The intensity of postoperative pain was assessed using a visual analog scale (VAS) (0 represented no pain and 10 the worst pain ever experienced) at 15, 30, 60th minutes, and 2nd, 4th, 6th hours postoperatively. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01858402
Study type Interventional
Source Baskent University
Contact
Status Completed
Phase Phase 2
Start date December 2009
Completion date July 2011

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