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A study on the optimum bolus dose of alfentanil for laryngeal mask airway insertion when co-administered with a single standard dose of propofol in children

A study on the optimum bolus dose of alfentanil for laryngeal mask airway insertion when co-administered with a single standard dose of propofol in children

Status
Completed
Phases
Unknown
Study type
Observational
Source
ANZCTR
Registry ID
ACTRN12613000657729
Acronym
Nil
Enrollment
35
Registered
2013-06-14
Start date
2014-08-07
Completion date
2014-11-28
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

The use of the laryngeal mask airway in children has increased with increasing day-case surgery in paediatric patients. Successful insertion of the laryngeal mask requires adequate mouth opening and sufficient depth of anaesthesia to minimise the upper airway reflexes and to prevent the untoward events of coughing, gagging and laryngospasm. Although propofol is a commonly used induction agent due to its depressant effects on airway reflexes, propofol alone does not prevent undesirable airway responses.Consequently, a potent and short-acting opioid (for example alfentanil ) is often added to facilitate laryngeal mask insertion in adults with minimal haemodynamic changes.However, the optimal bolus dose of alfentanil for children in this context has not been established. This study was designed, therefore, to determine the optimal dose of alfentanil required for the successful insertion of the laryngeal mask airway with a single bolus dose of propofol at induction (2.5 mg/kg)without a neuromuscular blocking agent in children.

Interventions

A predetermined bolus dose of alfentanil was injected over 30 seconds, followed by propofol 2.5 mg/kg over 10 seconds. The bolus dose of alfentanil was determined by a modified Dixon’s up-and-down method, starting from 10 microg/kg (2microg/kg as a step size). Laryngeal mask insertion was attempted 90 seconds after the end of alfentanil injection and the response of patients was classified as either ‘success’ or ‘failure’.

Sponsors

Yusheng Yao
Lead SponsorIndividual

Eligibility

Sex/Gender
All
Age
3 Years to 7 Years
Healthy volunteers
No

Inclusion criteria

ASA 1 and 2 patients of either gender of the age 3- 7 years undergoing elective surgery under general anaesthesia which can be performed with LMA insertion

Exclusion criteria

airway malformations, clinical evidence of patients with difficult airway, asthma or any sign of upper respiratory tract infection.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026