Effect of respiratory tidal volume on the required dose of remifentanil to create controlled hypotensio
Phase 2
- Conditions
- Rhinoplasty.Other and unspecified disorders of nose and nasal sinuses
- Registration Number
- IRCT20200825048515N71
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Candidate patients for rhinoplasty
Age group 18-65 years
Weight more than 50 kg
American Society of Anesthesiologists (ASA) class is equal to I
Informed consent to participate in the study
Exclusion Criteria
Being addicted to opioid products
Having the comorbidity (such as respiratory and coagulation disease)
History of allergy to the studied drug
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Blood pressure. Timepoint: Before surgery, immediately before anesthesia and every 10 minutes during surgery until the end of surgery. Method of measurement: Monitoring device.;Blood pressure. Timepoint: Before surgery, immediately before anesthesia and every 10 minutes during surgery until the end of surgery. Method of measurement: Monitoring device.;Satisfaction. Timepoint: End of surgery. Method of measurement: Visual Analogue Scale (VAS).
- Secondary Outcome Measures
Name Time Method