Evaluation of the effect of endotracheal intubation and laryngeal mask on respiratory parameters
Phase 3
Recruiting
- Conditions
- Orthopedic patients.Orthopedic aftercare
- Registration Number
- IRCT20220612055153N1
- Lead Sponsor
- Bandare-abbas University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 96
Inclusion Criteria
Patients aged 18 to 70 years ASA I, II candidate for elective orthopedic surgery under general anesthesia
Exclusion Criteria
History of COPD, asthma, ILD, and pulmonary fibrosis with active lung infection
EF fraction (less than ?40%)
BMI > ?35 kg / m2
Emergency surgery
Airway malformation
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Investigation of respiratory parameters. Timepoint: Evaluation of respiratory parameters at 1, 3, 5, 10 and 15 minutes after airway establishment. Method of measurement: Measurement of arterial oxygen saturation percentage by pulse oximetry device and End-tidal carbon dioxide(Etco2) via capnograph.
- Secondary Outcome Measures
Name Time Method Respiratory complications during surgary. Timepoint: Measurement of respiratory parameters such as blood oxygen saturation percentage (spo2) and end-tidal carbon dioxide (Etco2) at 1, 3, 5, 10 and 15 minutes after establishing airway. Method of measurement: Pulse oximetry and capnography device.