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Comparison of postoperation complication between Laryngeal Mask Airway and Endotracheal tube during low flow anesthesia with controlled ventilation

Comparison of postoperation complication between Laryngeal Mask Airway and Endotracheal tube during low flow anesthesia with controlled ventilation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201203042582N5
Enrollment
80
Registered
2012-03-15
Start date
2012-01-30
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

dysphagia. dysphagia

Interventions

Intervention 1: interventiobn group: insertion of LMA. Intervention 2: control group: insertion of endotracheal tube.
Treatment - Other
interventiobn group: insertion of LMA
control group: insertion of endotracheal tube

Sponsors

research chancellor, tabriz university of medical sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: adult patients with ASA class I and II aging 20-60 years who are candidates for elective surgery Exclusion criteria: possibility of air way problems, history of recent sore throat or a cold in the past 10 days, patients with latex allergy, patients with full stomach

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Sore throat. Timepoint: every 6 hours until 24 hours. Method of measurement: asking from patient.;Cough. Timepoint: every 6 hours until 24 hours. Method of measurement: asking from patient.

Secondary

MeasureTime frame
Dysphagia. Timepoint: every 6 hours until 24 hours. Method of measurement: asking from patient.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAfsaneh Mohammadi

tabriz university of medical sciences

afsanehmohammadi@yahoo.com+98 41 1657 7340

Outcome results

None listed

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