Comparison of the effect of lidocaine- paracetamol with lidocaine- ketamine on post-tonsillectomy pain relief in children

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20221127056627N2

Enrollment

114

Registered

2024-09-18

Start date

2024-10-01

Completion date

Unknown

Last updated

2025-01-08

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): After selection of target group, ampoule of lidocaine with a dose of 1 mg/kg will be prepared as Similar syringes 10 cc plus Paracetamol 15 mg/kg .This solutio

Eligibility

Sex/Gender

All

Age

3 Years to 10 Years

Inclusion criteria

Inclusion criteria: Patients with ASA grade I or II (American Society of Anesthesiology classification) Patients between 3 and 10 years old Patients undergoing open tonsillectomy

Exclusion criteria

Exclusion criteria: Allergy to the drugs used in the study significant cognitive impairment in children Positive history of Heart, kidney diseases and chronic pain. Lack of parental consent

Design outcomes

Primary

Measure	Time frame
Pain after surgery. Timepoint: 15, 30 and 45 minutes after surgery in recovery. Method of measurement: Wong-Baker Pain Scale.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahsa Jalilpoura gdam

Shiraz University of Medical Sciences

mahsa.jalilpour@yahoo.com0987136474270

Outcome results

None listed

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