Comparison of the clinical performance of i-gel™ and LMA Supreme™ in anesthetized geriatric patients

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

CRIS

Registry ID

KCT0002674

Enrollment

Registered

2018-02-02

Start date

2017-11-22

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 : All patients were arrived at operating room without premedication. Routine monitoring including pulse oximetry, non-invasive automated blood pressure monitoring, electrocardiography,

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1) 65 ~ 85 year old 2) patients undergoing elective surgery which is expected ending within 2 hours 3) American Society of Anesthesiologist Patient Status I~III

Exclusion criteria

Exclusion criteria: 1) emergency operation 2) uncontrolled hypertension(systlic blood pressure before anesthesia induction = 180mmHg) 3) obesity (Body mass index >35kg/m2) 4) pharyngeal pathology 5) risk of gastroespophageal reflux 6) end stage renal disease 7) respiratory disease 8) wobbling teeth 9) psychiatric disease or cognitive disorder

Design outcomes

Primary

Measure	Time frame
device insertion time for succeful ventilation	—

Secondary

Measure	Time frame
success rate in first attempt	—

Countries

Korea, Republic of

Contacts

Public ContactTae-Yun Sung

Konyang University Hospital

unt1231@naver.com+82-42-600-9317

Outcome results