The effect of remifentanil on endotracheal intubatio
Not Applicable
- Conditions
- In the absence of muscle relaxants to facilitate intubation.Failed or difficult intubation
- Registration Number
- IRCT201110216803N2
- Lead Sponsor
- Mazandaran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 162
Inclusion Criteria
Informed written consent; ASA class ?-??; Age between 18 and 50 years; Elective surgery; Mallampati class ?-??.
Exclusion criteria: History of difficult intubation; Pulmonary diseases; Recent respiratory tract infection; History of previous surgery on the larynx; Smoking; Gastroesophageal reflux; Hiatal hernia; Substance abuse; Pregnancy; Obesity; Renal diseases (baseline serum creatinine > 2mg/dl); Hepatic diseases (liver function tests > 1.5 times of the normal upper limit).
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Tracheal intubation. Timepoint: 90 seconds after induction of anesthesia. Method of measurement: on the movement and position of vocal cord, airway reaction and limb movement as excellent, good and poor will be assessed.
- Secondary Outcome Measures
Name Time Method Systolic pressure. Timepoint: Immediately and 5 min after laryngoscopy and tracheal intubation. Method of measurement: manometer.;Diastolic pressure. Timepoint: Immediately and 5 min after laryngoscopy and tracheal intubation. Method of measurement: manometer.;Heart rate. Timepoint: Immediately and 5 min after laryngoscopy and tracheal intubation. Method of measurement: manitoring.