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Study on appropriate size choice of supraglottic device, i-jel

Study on appropriate size choice of supraglottic device, i-jel - Appropriate size choice of i-jel

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000034041
Enrollment
400
Registered
2018-11-07
Start date
2018-02-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

The adult patients who undergo general anesthesia

Interventions

None listed

Sponsors

Shikoku Central Hospital
Lead Sponsor
IMS Fujimi General Hospital
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The adults who require airway maintenance by a supraglottic device for general anesthesia

Exclusion criteria

Exclusion criteria: The patients who have been already performed endotracheal intubation, the patients with the disease in the respiratory tract, the patients who judged that a study person in charge was inadequate.

Design outcomes

Primary

MeasureTime frame
Reak pressure, airway pressure

Secondary

MeasureTime frame
Trachea fiber findings, presence or absence of change to endotracheal intubation, the appliance which we used at endotracheal intubation, complications with the endotracheal intubation

Countries

Japan

Contacts

Public ContactShinji Kawahito

Shikoku Central Hospital Anesthesiology

kawahito.shinji@tokushima-u.ac.jp0896583515

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026