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Comparison of methods for selection of the appropriate size of LMA supreme in children

Comparison of methods for selection of the appropriate size of LMA supreme in children

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0002530
Enrollment
66
Registered
2017-11-10
Start date
2017-04-03
Completion date
Unknown
Last updated
2019-03-11

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

Conditions

None listed

Interventions

Medical Device : Regardless of participation in the study, all patients had the same pre-, mid-, and post-treatment and anesthetic procedures. Patients who were enrolled in the study were found to hav

Sponsors

Yonsei University Health System, Severance Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: - Children under 12 years of age who are able to use LMA Supreme 1.5 to 3 under general anesthesia under the general anesthesia and who are in the borderline region of the reference weight (standard weight ± 2.0 kg) - Patients who underwent surgery under general anesthesia. The type, scope, and duration of surgery were maintained by LMA Supreme when anesthesiologists and surgical surgeons were able to maintain airway. - It is not known to which group the research participant is assigned. - Method of extracting subjects: non-probabilistic

Exclusion criteria

Exclusion criteria: - If you have an anatomical structure that is suspected to be difficult to mask respiration or intubation, or if you have a history of it - In case of respiratory disease - If there is insufficient fasting time (6 hours for milk powder, 4 hours for breast milk) or if there is a risk of aspiration such as gastroesophageal reflux

Design outcomes

Primary

MeasureTime frame
Failure to insert and improper ventilation

Secondary

MeasureTime frame
The subject's weight (kg)

Countries

Korea, Republic of

Contacts

Public Contacthyo-jin byon

Yonsei University

jinoben@naver.com+82-2-2228-2429

Outcome results

None listed

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