the survey of pain injection of propofol
Phase 2
- Conditions
- Pain severity induced by propofol injection.
- Registration Number
- IRCT2012072310340N1
- Lead Sponsor
- Vice chancellor for research, Golestan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 257
Inclusion Criteria
inclusion criteria: patient fully satisfied to be studied,between 15-55years-old and ASA1,2
exclusion criteria:A history of drug abuse, alcohol or taking any pain medication during 24 hours before surgery, a history of neurological disease, chronic pain syndrome, thrombofelebit, advanced systemic disease (such as advanced diabetes), and any contraindication based on injection of Propofol lead to patient withdrawal from the study
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: 24 houre after end of surgery. Method of measurement: Visual analog scale.
- Secondary Outcome Measures
Name Time Method