Effects of propofol infusion with and without lidocaine on pain and need for sedation during ERCP
Phase 2
Recruiting
- Conditions
- Pain.Acute pain, not elsewhere classifiedG89.1
- Registration Number
- IRCT20190325043107N33
- Lead Sponsor
- Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
ASA class I to III patients
ERCP candidate
Exclusion Criteria
Patients with arterial oxygen saturation less than 90%
Heart rate less than 50
Seizure patients
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: Once every 10 minutes and for thirty minutes. Method of measurement: Visual Analogue Scale.
- Secondary Outcome Measures
Name Time Method Sedation. Timepoint: For a moment and for thirty minutes. Method of measurement: Patient observation.