Effect of Lidocaine Pretreatment on Propofol Injection Pain During Upper Gastrointestinal Endoscopy
Not Applicable
Completed
- Conditions
- Diseases of the digestive system
- Registration Number
- KCT0000045
- Lead Sponsor
- Keimyung University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 66
Inclusion Criteria
Patients, 16 - 80 year-old, scheduled to undergo sedative diagnostic upper GI endoscopy
Exclusion Criteria
(1) those who were pregnant, (2) those who were allergic to soybeans, eggs or any drugs, (3) those who received sedatives or analgesics within 24 hours before the procedure, (4) those with poor general condition who had an American Society of Anesthesiology classification = 3 and (5) those who had psychiatric disorders or arrhythmia (6) those who had invisible dorsal hand vein for cannulation
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method pain score (severity of pain perception)
- Secondary Outcome Measures
Name Time Method remembrance of pain