Effective Dose of Alfentanil Combined With Propofol for Laryngeal Mask Airway Insertion in Children

Trial statusNot yet recruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age7-12
SponsorZhongshan Ophthalmic Center, Sun Yat-sen University

About this trial

This study uses a prospective, up-and-down sequential allocation method to determine the median effective dose (ED50) and 95% effective dose (ED95) of alfentanil combined with propofol for successful laryngeal mask airway (LMA) insertion in children aged 7-12 undergoing elective day surgery.

Eligibility criteria

Qualifiers

Aged 7 to 12 years

Undergoing elective day surgery

ASA physical status I-II

Body Mass Index (BMI) between 14 and 24 kg/m²

Disqualifiers

Allergy to opioids

Unresolved upper respiratory tract infection within the past 1 week

Abnormal heart, lung, liver, or kidney function, or metabolic diseases

Airway anatomical abnormalities (e.g., micrognathia, laryngomalacia, macroglossia) or OSAHS (Obstructive Sleep Apnea-Hypopnea Syndrome)

Trial design

Treatments tested in this trial

  • Alfentanil

Treatment groups

40 Participants
are divided into 1 treatment group