The effect of Tramadol on postoperation pain control in children undergoing Tonsillectomy and Adenotonsillectomy
Not Applicable
- Conditions
- Acute pain.Acute pain
- Registration Number
- IRCT2013082014199N3
- Lead Sponsor
- Research Council of Iran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Other
- Sex
- All
- Target Recruitment
- 72
Inclusion Criteria
Children aged 4-10 years old, who were in ASA physical status classification and have been placed in groups I and II, and they were candidates for tonsillectomy with or without adenoidectomy. Exclusion criteria: Sensitivity to opioids or local anesthetics, contraindication opioids or local anesthetics, Asthma, kidney disease, liver disease, throat infections, coagulation disorders
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Acute pain. Timepoint: At 0(Recovery), 2, 4, 6, 12, 18 and 24 hours after the operation and 7 days after that. Method of measurement: wong Baker visual scale.
- Secondary Outcome Measures
Name Time Method ausea and Vomiting. Timepoint: At 0(Recovery), 2, 4, 6, 12, 18 and 24 hours after the operation and 7 days after that. Method of measurement: Observation.;Bleeding. Timepoint: At 0(Recovery), 2, 4, 6, 12, 18 and 24 hours after the operation and 7 days after that. Method of measurement: Observation.