Clinical Trials Directory

Trials / Completed

CompletedNCT01858402

Paracetamol Versus Dipyrone After Pediatric Lower Abdominal Surgery in Children With Spinal Anesthesia

The Efficacy of Intravenous Paracetamol Versus Dipyrone for Postoperative Analgesia After Day-case Lower Abdominal Surgery in Children With Spinal Anesthesia: a Prospective Randomized Double-blind Study

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
2 (actual)
Sponsor
Baskent University · Academic / Other
Sex
All
Age
8 Years – 15 Years
Healthy volunteers
Accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
DRUGParacetamol15 mg/kg IV (premixed with 0.9% sodium chloride to a total of 50 ml), preoperative single dose
DRUGDipyrone15 mg/kg IV (premixed with 0.9% sodium chloride to a total of 50 ml), preoperative single dose

Timeline

Start date
2009-12-01
Primary completion
2011-03-01
Completion
2011-07-01
First posted
2013-05-21
Last updated
2013-05-21

Source: ClinicalTrials.gov record NCT01858402. Inclusion in this directory is not an endorsement.