CompletedPhase 2

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

2 participantsStarted 2009-12

Plain-language 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.

Who can participate

Age range8 Years – 15 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * American Society of Anesthesiologist (ASA) physical status I and II children undergoing elective lower abdominal surgery Exclusion Criteria: * increased intracranial pressure hemorrhagic diathesis infection at the puncture site Those with a known history of allergy to the study drugs

What they're measuring

Change from pain intensity until postoperative 6 hours

Timeframe: Pain intensity recorded until postoperative 6 hours

Trial details

NCT IDNCT01858402

SponsorBaskent University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2011-03

View on ClinicalTrials.gov More Other Acute Postoperative Pain trials