Investigating the effect of Lidocaine and Dexmedetomidine on Tonsillectomy

Comparing the effectiveness of Lidocaine and Dexmedetomidine on the severity of immediate complications after Tonsillectomy surgery

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20160307026950N49

Enrollment

Registered

2022-12-23

Start date

2023-01-05

Completion date

Unknown

Last updated

2023-02-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tonsillectomy. Chronic tonsillitis

Interventions

Intervention 1: Intervention group A: patients 10 minutes before anesthesia, receive 1.5 mg/kg lidocaine 2% (manufactured by Aburihan company) intravenously within 10 minutes, followed by an intraveno

Eligibility

Sex/Gender

All

Age

4 Years to 12 Years

Inclusion criteria

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

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

Design outcomes

Primary

Measure	Time frame
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.	—

Measure

Time frame

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.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactShima Shams

Esfahan University of Medical Sciences

shimashams9776@gmail.com+98 31 3620 2020

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026