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
| Type | Name | Description |
|---|---|---|
| DRUG | Paracetamol | 15 mg/kg IV (premixed with 0.9% sodium chloride to a total of 50 ml), preoperative single dose |
| DRUG | Dipyrone | 15 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.