Investigating the effect of Lidocaine and Dexmedetomidine on Tonsillectomy

Phase 3

Recruiting

• Conditions: Tonsillectomy.; Chronic tonsillitis; J35.01

• Registration Number: IRCT20160307026950N49
• Lead Sponsor: Esfahan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 7 February 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 90

Inclusion Criteria

Patients 4 to 12 years old
Anesthesia class I and II according to ASA criteria
Candidate for tonsillectomy surgery
Informed consent to enter the study

Exclusion Criteria

The presence of acute respiratory infections
Abnormal coagulation tests
History of allergic to drugs used

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Bleeding rate. Timepoint: From the start of surgery to 6 hours after surgery. Method of measurement: Based on the examination of the number, weight and percentage of blood gases and the amount of blood in the suction device.;Laryngospasm. Timepoint: During the first two hours after the operation. Method of measurement: Based on the observation of signs of acute respiratory obstruction.;Laryngitis. Timepoint: In the first 24 hours after the operation. Method of measurement: Based on the observation of hoarseness and snoring.