Comparison the effects of acetaminophen on pain control after adenotonsillectomy in childre

Phase 1

• Conditions: adenotonsillectomy.; Nasopharynx; T 17.2

• Registration Number: IRCT201107301138N8
• Lead Sponsor: Guilan University of Medical Sciences, Vice Chancellor for Research

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 96

Inclusion Criteria

patirnts candidate for elective adenotonsillectomy surgery (4 – 10 yr); ASA claa I , II
Exclusion criteria:emergency surgery; history of the known sensitivity to acetaminophen; history of liver, renal, respiratory , cardiac diseases, seizure; history of chronic pain with usage of analgesics

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Post operative pain. Timepoint: from beginning of recovery every 15 minutes , in the first 6 hours every 2 hours then up to 24 hours, every 6 hours. Method of measurement: With table.

Secondary Outcome Measures

Name	Time	Method
Agitation. Timepoint: from beginning of post anesthesia car unit every 15 minutes , in the first 6 hours every 2 hours, then up to 24 hours, every 6 hours. Method of measurement: With scoring table.