To investigate whether there is an effect of decreasing vascular pain in propofol injection when warming the forearm
Not Applicable
- Conditions
- Not Applicable
- Registration Number
- KCT0002293
- Lead Sponsor
- Chungnam National University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
americal society of anesthesiologist physical status I-II , aged 18yrs~65yrs patients scheduled for emergency or elective surgery written informed consent
Exclusion Criteria
Patients pregnant and breastfeeding, children, Significant cardiovascular disease, kidney disease, liver disease, neurological deficit, Psychiatric illness, Patients with difficult communication, local anesthetics(lidocaine) anaphylaxis or allergy, Skin diseases on the back of the hand, Redness, swelling, Patients using topical analgesics, Patients taking aspirin and clopidogrel
Study & Design
- Study Type
- Observational Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method when propofol was administered only 25% of the total amount of propofol (2 mg / kg), we assess the degree of pain in the patient.
- Secondary Outcome Measures
Name Time Method whether patients who was unconscious respond to the pain during we inject rocuronium 0.6 mg intravenously or not.