Comparison of propofol or isofluran anesthesia for sinus surgery
Phase 2
- Conditions
- Chronic Sinusitis.Chronic sinusitis, unspecified
- Registration Number
- IRCT201102081138N7
- Lead Sponsor
- Guilan University of Medical Sciences, Vice Chancellor for Research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 44
Inclusion Criteria
Patients candidated for elective endoscopic sinus surgery (15-45yr); ASA class I,II; Patients with completely treated nose and sinus infections
Exclusion criteria:
History of hemorrhagic disease; Seizure; Drugs that affect on the surgical homeostasis; Anemia (Hb <10); Poor controlled cerebrovascular accident; History of significant CAD; Arrhythmia; Liver or kidney dysfunction; Electrolyte or metabolic abnormalities; COPD; Severe asthma or other severe respiratory disease; History of PUD; Pregnancy
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Surgical field condition. Timepoint: Every 15 minutes. Method of measurement: With table.
- Secondary Outcome Measures
Name Time Method Intraoperative bleeding percent. Timepoint: Every 15 minutes Intraoperatively. Method of measurement: Maximum allowable blood loss formula.