Status:
COMPLETED
Paracetamol Versus Dipyrone After Pediatric Lower Abdominal Surgery in Children With Spinal Anesthesia
Lead Sponsor:
Baskent University
Conditions:
Other Acute Postoperative Pain
Eligibility:
All Genders
8-15 years
Phase:
PHASE2
Brief 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 child...
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 posto...
Eligibility Criteria
Inclusion
- American Society of Anesthesiologist (ASA) physical status I and II children undergoing elective lower abdominal surgery
Exclusion
- increased intracranial pressure hemorrhagic diathesis infection at the puncture site Those with a known history of allergy to the study drugs
Key Trial Info
Start Date :
December 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 1 2011
Estimated Enrollment :
2 Patients enrolled
Trial Details
Trial ID
NCT01858402
Start Date
December 1 2009
End Date
July 1 2011
Last Update
May 21 2013
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