idocaine for reducing pain from intravenous Nefopam infusio
Phase 4
Completed
- Conditions
- pain from nefopam injectionpain,nefopam,vascular pain
- Registration Number
- TCTR20201125006
- Lead Sponsor
- none
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 42
Inclusion Criteria
General Patient age 20-80 years old who was schedile for an elective surgery at King Chulalongkorn Memorial Hospital with a plan for regional anesthesia (Neuraxial/peripheral anesthesia)
Exclusion Criteria
1.Patient allergy to any medication used in the study
2.Patient unable to state or understand VAS score
3.Patient who had previous experience with nefopam
4.Patient with Chronic pain
5.Patient who was having medication which increase Serotonin level
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method pain from nefopam decreased with lidocaine infusion 5 minutes VAS pain score
- Secondary Outcome Measures
Name Time Method pain from nefopam decreased with lidocaine infusion 1, 10 and 15 minutes VAS pain score