Comparison of the effects of using supraglottic airway and classic laryngeal mask among children underwent surgery

Comparison of the effects of using supraglottic airway and classic laryngeal mask among children underwent surgery with general anesthesia

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT2016091726858N4

Enrollment

Registered

2016-10-08

Start date

2016-09-22

Completion date

Unknown

Last updated

2018-02-22

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

Conditions

Condition 1: hernia. Condition 2: hydrocele. Inguinal hernia, Bilateral inguinal hernia, with obstruction, without gangrene, Bilateral inguinal hernia, with gangrene, Bilateral inguinal hernia, without obstruction or gangrene, Unilateral or unspecified inguinal hernia, with obstruction, without gang hydrocele of spermatic cord, testis or tunica vaginalis

Interventions

Intervention 1: Intervention group: in the proper depth of anesthesia, appropriate size of supraglottic airway based on the child weight and the manufacturer's instructions will be selected and placed

Prevention

Intervention group: in the proper depth of anesthesia, appropriate size of supraglottic airway based on the child weight and the manufacturer's instructions will be selected and placed by an anesthesi

Control group: in the proper depth of anesthesia, appropriate size of classic laryngeal mask based on the child weight and the manufacturer's instructions will be selected and placed by an anesthesiol

Eligibility

Sex/Gender

All

Age

6 Months to 5 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: the age of six months to six years; elective hernia or hydrocele surgery in supine position; no respiratory diseases and airway problems; no obstructive sleep apnea; no regurgitation; non-emergency surgery; no history of surgery on the abdomen and chest and BMI less than 30. Exclusion criteria: problems during surgery; problems during tracheal intubation and prolonged surgery (more than one hour).

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Maximum airway pressure. Timepoint: Intraoperative. Method of measurement: Ventilator.;Blood on equipment. Timepoint: Intraoperative. Method of measurement: Observation.;Sore Throat. Timepoint: Postoperative. Method of measurement: Interviews with patients.;End-Tidal CO2. Timepoint: Intraoperative. Method of measurement: Ventilator.;Cough. Timepoint: Postoperative. Method of measurement: Observation and interviews with patients.;Nausea. Timepoint: Postoperative. Method of measurement: Interviews with patients.;Vomit. Timepoint: Postoperative. Method of measurement: Interviews with patients.;Shortness of breath. Timepoint: Postoperative. Method of measurement: Interviews with patients.;Dysphagia. Timepoint: Postoperative. Method of measurement: Interviews with patients.	—

Measure

Time frame

Maximum airway pressure. Timepoint: Intraoperative. Method of measurement: Ventilator.;Blood on equipment. Timepoint: Intraoperative. Method of measurement: Observation.;Sore Throat. Timepoint: Postoperative. Method of measurement: Interviews with patients.;End-Tidal CO2. Timepoint: Intraoperative. Method of measurement: Ventilator.;Cough. Timepoint: Postoperative. Method of measurement: Observation and interviews with patients.;Nausea. Timepoint: Postoperative. Method of measurement: Interviews with patients.;Vomit. Timepoint: Postoperative. Method of measurement: Interviews with patients.;Shortness of breath. Timepoint: Postoperative. Method of measurement: Interviews with patients.;Dysphagia. Timepoint: Postoperative. Method of measurement: Interviews with patients.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatihe Kerman Saravi

Zahedan University of Medical Sciences

f_kermansaravi@yahoo.com+98 54 3341 1415

Outcome results

None listed

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