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The effect of acetaminophen to reduce pain in tonsillectomy

Not Applicable
Conditions
Hypertrophy of tonsils and adenoids.
Hypertrophy of tonsils with hypertrophy of adenoids
Registration Number
IRCT2015083023811N1
Lead Sponsor
Deputy of Research and Technology
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
100
Inclusion Criteria

children undergoing adenotonsillectomy?children 7_15 years with recurrent tonsillitis?chronic tonsillitis?obstructive sleep apnea syndrome?open mouth breathing?snoring and dysphagia;Exclusion criteria: known allergy to acetaminophen?renal or hepatic dysfunction?use of pain killers during the past 24 hours?drug abuse (due to the high prevalence in the region)? known Favism disease?diarrhea?dehydration?bleeding disorders and act surgery lasted more than 30 minutes.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: 2 hours, 6 hours, 12 hours and 24 hours after intervention. Method of measurement: visual annalog pain scale.
Secondary Outcome Measures
NameTimeMethod
The need for pain medication after surgery. Timepoint: Every 1 hour after intervention. Method of measurement: Frequency of consumption.
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