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Comparison of postoperative respiratory complications of Laryngeal Mask Airway and Tracheal tube in candidates of prolonged ENT operations

Comparison of postoperative respiratory complications of Laryngeal Mask Airway and Tracheal tube in candidates of prolonged ENT operations

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013102215108N1
Enrollment
171
Registered
2014-01-03
Start date
2012-04-20
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

Respiratory complications of airway control devices. -injury, poisoning and certain other consequences of external causes

Interventions

Intervention 1: Intervention group: Laryngeal Mask Airway will be used. This was done using classic method without any introducer by Anesthesiology specialist trainees. Intervention 2: Control group:
Treatment - Devices
Intervention group: Laryngeal Mask Airway will be used. This was done using classic method without any introducer by Anesthesiology specialist trainees
Control group: Endotracheal intubation by anesthesiology specialist trainees

Sponsors

Vice Chancellor For research, Iran university of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: Inclusion criteria: ASA I and II patients; candidates for ENT surgeries of more than two hours duration; age more than 13y old; mallampati score of 1 or 2; no positive history of chronic or acute respiratory diseases or smoking; Exclusion criteria: Obese patients; pregnant women; patients with gastroesophageal reflux; patients with surgeries on throat and lower regions of respiratory system

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Sore Throat. Timepoint: 2 hours after operation. Method of measurement: Asking from the patient.;Hoarsness. Timepoint: 2 hours after operation. Method of measurement: Asking from the patient.;Cough. Timepoint: 2 hours after operation. Method of measurement: Asking from the patient.;Shortness of breath. Timepoint: 2 hours after operation. Method of measurement: Asking from the patient and direct observation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactReza Safaeian

Iran University of Medical Sciences

rezasafaa@hotmail.com+98 21 4464 0531

Outcome results

None listed

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