A STUDY INTENDED TO FIND THE ADEQUACY OF VARIOS DOSES OF FENTANYL BEFORE ANAESTHESIA IN ACHIEVING DESIRED HYPOTENSIO
Not Applicable
Completed
- Conditions
- Health Condition 1: J324- Chronic pansinusitisHealth Condition 2: null- Patients with rhinosinusitis undergoing Functional endoscopic sinus surgery
- Registration Number
- CTRI/2014/03/004457
- Lead Sponsor
- Department of Anaesthesiology Pain Perioperative Medicine Sir Ganga Ram Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 120
Inclusion Criteria
1. ASA physical status grade I-II
2. Patients scheduled to undergo bilateral FESS involving non-fungal sinusitis under general anaesthesia (GA)
Exclusion Criteria
Uncontrolled hypertension
Hepato-renal disease
Hypersensitivity to opioids
Associated cranio-facial anomaly
Significant cardio-vascular disease
Psychiatric disorders
Pre-existing hyper-reactive airways disease
Chronic alcoholics and/or smokers
Inability to attain/sustain induced hypotension
Hyperactive response to fentanyl (apnea, hypotension
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Achievement and maintenance of intraoperative induced hypotensionTimepoint: From induction of anaesthesia to end of surgery
- Secondary Outcome Measures
Name Time Method 1. Improvement in surgical field conditions <br/ ><br> 2. Intraoperative propofol-sparing effect <br/ ><br> 3. Frequency of intra-operative specific hypotensive supplements (if any)to anaesthesia (propofol TIVA) and analgesia (fentanyl) <br/ ><br>4. Postoperative outcome (side effects, awakening)Timepoint: From induction of anaesthesia to 24 hrs postoperatively