Effect of sevoflurane and propofol for laryneal mask airway insertion

Comparison of sevoflurane with and without propofol for laryneal mask airway insertion in children; a double-blinded clinical trial

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20201207049639N5

Enrollment

Registered

2021-01-09

Start date

2020-06-22

Completion date

Unknown

Last updated

2021-02-22

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

Conditions

Laryneal mask airway insertion in children.

Interventions

Intervention 1: Intervention group: Patients in the intervention group underwent induction of anesthesia with 8% sevoflurane with oxygen and N2O in equal proportions. The criterion of anesthesia was t

Eligibility

Sex/Gender

All

Age

2 Years to 8 Years

Inclusion criteria

Inclusion criteria: Age between 2 to 8 years old American Society of Anesthesiologists (ASA) I and II Abdominal and lower limb surgeries

Exclusion criteria

Exclusion criteria: Dissatisfaction of parents to participate in the study Possibility of surgery with spinal anesthesia

Design outcomes

Primary

Measure	Time frame
Time to reach the desired relaxation for laryngeal mask insertion. Timepoint: Due to the nature of the variable under study, which is time, only once from the time of administration of sevoflurane to the desired relaxation was considered. Method of measurement: Timer by second.	—

Secondary

Measure	Time frame
Heart rate. Timepoint: Once during laryngeal mask insertion. Method of measurement: Pulsoximeter.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Hadi Hooshyar

Oroumia University of Medical Sciences

hooshyar.h@umsu.ac.ir+98 44 3198 8293

Outcome results

None listed

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