Efficacy of local anaesthesia of bupivacaine in combination with tramadol in post adenotonsillectomy pai
Not Applicable
- Conditions
- Condition 1: Local anaesthetics. Condition 2: Acute pain.Local anaestheticsAcute pain
- Registration Number
- IRCT201308035362N8
- Lead Sponsor
- Isfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 120
Inclusion Criteria
5 to 15 years old who were candidate for tonsillectomy with or without adenoidectomy;
exclusion criteria: patients with acute pharyngeal infection; allergy to bupivacaine or tramadol; acute and active infection of respiratory tract with fever and rhonchi; constant use of sedative or analgesic hypnotic; peritonsillar abscess; renal disease; liver disease; asthma and coagulation disorders.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: Time of 0,15,30,60 minutes in recovery and 4,8,16,28 hour in ward. Method of measurement: ops (objective pain scale).
- Secondary Outcome Measures
Name Time Method Consciousness level. Timepoint: Time of 0,15,30,60 minutes in recovery and 4,8,16,24 hours in ward. Method of measurement: Watching in 4 grading.;Mean blood pressure - mean heart rate. Timepoint: Time of 0,10,30,60 minutes in operation and 0,30,60 minutes in recovery. Method of measurement: Monitoring.;Nausea and vomiting. Timepoint: After operation to 24 hours. Method of measurement: Watching.;Mean time to awaking. Timepoint: after operation. Method of measurement: Watching.;Mean first time to asking analgesic. Timepoint: After operation to 24 hours. Method of measurement: Watching.;Mean time to extubation. Timepoint: after operation. Method of measurement: Watching.