Comparative study of EMLA cream and lidocaine tape on the reduction of the pain at venipunture
Not Applicable
- Conditions
- Patients who receive general anesthesia
- Registration Number
- JPRN-UMIN000023030
- Lead Sponsor
- Tomakomai city hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 24
Inclusion Criteria
Not provided
Exclusion Criteria
Past history of allergy for local anesthetics. Past history of contact dermatitis. Dermal abnormality on the puncture sites. Severe hepatic, renal or cardiovascular disease. Methemogulobinemia Porphyria Pregnancy or lactation period Communication difficulty Sensory disturbance Anesthesiologist or attending physician determine that the patient is inappropriate for this study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Visual Analogue Scale(VAS)
- Secondary Outcome Measures
Name Time Method Verbal Rating Scale(VRS), adverse event