Oxygen at higher flow rates during endoscopy procedure
Not Applicable
- Conditions
- Health Condition 1: null- Patients admitted in the hospital and scheduled for elective ERCP procedure under sedation will be trial participants.
- Registration Number
- CTRI/2017/08/009248
- Lead Sponsor
- RAKHEE GOYA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. ASA I-III
2. BMI <35 kg/m2
3. Scheduled for elective ERCP under sedation
Exclusion Criteria
1. Pre-existing respiratory impairment or coronary artery disease
2. anticipated difficult airway
3. pregnancy
4. allergy to any of the study drugs
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method umber of episodes of desaturation (SpO2 less than 90% for 10 sec) during propofol-fentanyl based sedation for ERCPTimepoint: Number of episodes of desaturation (SpO2 less than 90% for 10 sec) during propofol-fentanyl based sedation for ERCP
- Secondary Outcome Measures
Name Time Method adverse effects in postoperative roomTimepoint: 5min, 10min, 15min, 20 min, 25 min, 30 min;level of endoscopistâ??s satisfactionTimepoint: 90 min;number of endoscope removal and reinsertionsTimepoint: 90 min;patient satisfactionTimepoint: 6 hours;total propofol consumptionTimepoint: 90 min