Child
Conditions
Interventions
This is a randomized controlled trial with four arms, double-blind. A total of 120 eligible individuals will be randomly allocated to one of the intervention groups using a randomization program from
Sponsors
Faculdade de Ciências Médicas e da Saúde da Pontifícia Universidade Católica de São Paulo
Faculdade de Ciências Médicas e da Saúde da Pontifícia Universidade Católica de São Paulo
Eligibility
Age
2 Years to 10 Years
Inclusion criteria
Inclusion criteria: children aged 2 to 10; classified as American Society of Anesthesiologists (ASA) physical status I and II; undergoing general anesthesia for tonsillectomy with or without adenoidectomy
Exclusion criteria
Exclusion criteria: refusal to participate in the study; presence of renal disease; presence of hepatic disease; presence of neuromuscular disease; contraindication to the use of any of the drugs used in the study; body mass index equal to or greater than 30; acute clinical illnesses
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Determine if there is a significant difference in the time elapsed between Train of Four (TOF) 3 and 100% between the groups | — |
Secondary
| Measure | Time frame |
|---|---|
| To analyze whether the incidence of bradycardia, respiratory complications and postoperative nausea and vomiting has a significant difference between the groups | — |
Countries
Brazil
Contacts
Public ContactAntonio Moron Morad Neto
Faculdade de Ciências Médicas e da Saúde da Pontifícia Universidade Católica de São Paulo
Outcome results
None listed