The effect of continuous administration of two doses of sufentanil on changes in heart rate and blood pressure after laryngoscopy and tracheal intubatio
Phase 3
- Conditions
- Patients requiring tracheal intubation for general anesthesia.
- Registration Number
- IRCT20200825048515N62
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 90
Inclusion Criteria
Age range from 18 to 65 years
American Society of Anesthesiologists (ASA) I
Requires tracheal intubation for general anesthesia
Consent to participate in the study
Exclusion Criteria
Having heart failure
Having a systolic blood pressure of less than 14 mmHg and diastolic blood pressure of 9 mmHg
Having respiratory, liver, kidney failure
Having airway malformations
having an addiction
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Systolic blood pressure. Timepoint: Baseline time, before laryngoscopy, 1, 3, 10 minutes after laryngoscopy. Method of measurement: Ventilation device.;Diastolic blood pressure. Timepoint: Baseline time, before laryngoscopy, 1, 3, 10 minutes after laryngoscopy. Method of measurement: Ventilation device.;Heart beat. Timepoint: Baseline time, before laryngoscopy, 1, 3, 10 minutes after laryngoscopy. Method of measurement: Ventilation device.;Oxygen saturation (SPO2). Timepoint: Baseline time, before laryngoscopy, 1, 3, 10 minutes after laryngoscopy. Method of measurement: Ventilation device.
- Secondary Outcome Measures
Name Time Method